27775594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7048861-A-G

27785185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7051751-A-G

27785188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7051754-T-C

27785188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7051754-T-G

27785296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7051852-A-G

http://identifiers.org/hco/10/GRCh38#27785714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7052096-C-A

27785773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7052160-C-T

27787600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7054285-C-T

27795596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7063391-A-T

27795695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7063486-G-A

27795931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7063746-T-A

27795931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7063746-T-C

27795963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7063778-G-A

27795965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7063780-T-C

http://identifiers.org/hco/10/GRCh38#27796102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7063860-A-C

27796510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7064170-C-G

27796649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7064293-G-C

27796649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7064293-G-T

27796656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7064300-T-C

27796678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7064323-T-C

27796814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7064450-A-G

27796850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7064486-G-T

http://identifiers.org/hco/10/GRCh38#27796900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7064539-A-C

27796900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7064539-A-G

27797066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7064706-T-A

27797066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7064706-T-C

27797569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7065139-C-T

http://identifiers.org/hco/10/GRCh38#27797574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7065144-C-A

27797778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7065833-C-T

http://identifiers.org/hco/10/GRCh38#27797823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7065874-C-A

27799540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7067943-T-A

27799654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7068005-C-T

27799796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7068153-A-G

27799918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7068261-T-C

27800152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7068488-A-G

27800303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7068618-C-T

27800348-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7068653-T-A

http://identifiers.org/hco/10/GRCh38#27800547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7068927-A-C

27800619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7069000-T-C

27800877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7069268-G-A

27800877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7069268-G-T

27800886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7069277-A-G

27801193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7069573-G-A

27801193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7069573-G-C

27801588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7069972-C-T

27801651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7070020-C-T

27803467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7075925-G-A

http://identifiers.org/hco/10/GRCh38#27803594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7076043-C-A

27803594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7076043-C-T

27803612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7076061-C-T

27804000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7076763-G-T

27804090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7076855-G-A

27804090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7076855-G-T

27804287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7077012-T-G

27804624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7077362-G-A

27804659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7077399-T-C

27804824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7077545-C-T

27804825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7077546-C-T

27805106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7077821-G-C

27805319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7078007-G-A

27805407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7078083-C-T

http://identifiers.org/hco/10/GRCh38#27805893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7078150-A-C

27805920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7078176-T-G

27805964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7078200-G-A

27806054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7078272-T-G

http://identifiers.org/hco/10/GRCh38#27806536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7078472-A-C

27806536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7078472-A-T

27806705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7078638-C-T

27806711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7078644-A-G

27806753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7078680-G-T

27806808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7078735-T-C

27808255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7081064-A-G

27808356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7081149-G-A

27808541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7081313-C-T

27808997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7084377-T-C

http://identifiers.org/hco/10/GRCh38#27809652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7085768-A-C

http://identifiers.org/hco/10/GRCh38#27809860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7085972-A-C

http://identifiers.org/hco/10/GRCh38#27809908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7086020-C-A

27810089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7086180-T-C

27810323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7086363-C-T

27810535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7086541-C-T

27811327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7087276-G-A

http://identifiers.org/hco/10/GRCh38#27811504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7087465-C-A

27811692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7087660-A-T

27812071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7088025-G-T

27812089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7088043-C-T

http://identifiers.org/hco/10/GRCh38#27812099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7088053-A-C

http://identifiers.org/hco/10/GRCh38#27812103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7088057-C-A

27812103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7088057-C-T

http://identifiers.org/hco/10/GRCh38#27812353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7088304-C-A

27812445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7088396-T-C

http://identifiers.org/hco/10/GRCh38#27812491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7088436-C-A

27812499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7088441-G-A

27812499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7088441-G-T

27812596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7088538-G-A

27812596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7088538-G-T

http://identifiers.org/hco/10/GRCh38#27812635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7088578-A-C

27812727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7088664-T-A

27820150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7091756-T-G

27820364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7091952-A-T

27820400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7091989-C-T

http://identifiers.org/hco/10/GRCh38#27820416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7092005-A-C

27820441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7092013-A-G

http://identifiers.org/hco/10/GRCh38#27820752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7092262-C-A

27821214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7093959-G-A

27821214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7093959-G-T

27821641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7094390-G-A

27821641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7094390-G-C

27822743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7095464-G-A

27823088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7098926-G-C

27823121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7098959-G-T

http://identifiers.org/hco/10/GRCh38#27823378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7099164-C-A

27823550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7099326-T-C

27823625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7099391-A-G

27824774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7108368-A-G

27824797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7108390-T-C

27824855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7108438-G-T

27825169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7108781-T-C

27825221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7108828-T-C

27825231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7108842-G-C

27828080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7113187-T-C

27828254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7113333-G-A

27828478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7114591-T-G

27828683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7114991-A-G

27829072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7115275-T-C

27829229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7115420-C-T

http://identifiers.org/hco/10/GRCh38#27832235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7116452-C-A

27832266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7116483-G-A

27833335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7117558-G-A

27833533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7117737-G-T

27833662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7117864-T-C

27833759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7117942-G-T

http://identifiers.org/hco/10/GRCh38#27833950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7118194-A-C

27834019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7118262-G-C

27836730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7119050-T-C

27836801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7119124-T-C

http://identifiers.org/hco/10/GRCh38#27836871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7119197-A-C

27836871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7119197-A-G

http://identifiers.org/hco/10/GRCh38#27837431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7120508-C-A

27837431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7120508-C-T

27837529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7120605-T-C

27837540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7120620-C-G

27837574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7120655-G-T

27837633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7120714-T-C

27837725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7120804-G-A

27837777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7120833-T-G

http://identifiers.org/hco/10/GRCh38#27837810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7120851-C-A

27838365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7121079-T-G

27838883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7121611-C-T

27839287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7121986-C-T

27839444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7122140-G-C

27839447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7122143-T-A

27839460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7122155-A-G

27839716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7122398-A-G

27839723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7122405-T-C

27856108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7122608-C-T

27856240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7122710-T-G

27856261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7122736-A-G

27856261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7122736-A-T

27856542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7123023-T-G

27856560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7123040-T-C

27856569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7123049-C-G

27858551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7125259-T-C

http://identifiers.org/hco/10/GRCh38#27859105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7125574-A-C

27859346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7125814-T-C

27859440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7125907-G-C

27859505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7125970-T-C

27859577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7126036-A-G

27859733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7126369-T-C

27859810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7126443-C-G

27859984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7126628-T-A

27860174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7126797-G-A

27860727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 7127314-T-C

27860781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 7127368-A-G

27860928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7127477-A-T

http://identifiers.org/hco/10/GRCh38#27860941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7127490-C-A

27860941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7127490-C-G

27860941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7127490-C-T

27860944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7127493-T-A

27860944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7127493-T-C

27860964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7127507-A-G

27860986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7127529-T-C

27860989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7127532-T-G

27860995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7127538-G-T

27861419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7127878-G-T

27861444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7127907-A-G

27861699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7128701-T-C

27861723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7128720-C-T

27861970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7128955-G-T

27862104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129088-T-A

27862138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129118-T-C

27862138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129118-T-G

27862173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129150-G-A

27862244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129220-A-G

27862245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129221-T-A

27862245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129221-T-C

27862258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129234-G-A

27862264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129240-A-G

27862325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129302-G-T

27862362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129339-G-A

27862362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129339-G-T

27862736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129680-A-T

27862756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129700-T-C

27862952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129842-C-T

27862965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7129860-A-T

27863124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7130216-T-C

27863128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7130220-T-C

http://identifiers.org/hco/10/GRCh38#27863265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7130356-C-A

27863459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7130503-G-A

27863487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7130526-T-C

27863524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7130563-T-C

27863562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7130600-T-C

27877326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7135881-C-G

27877362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7135915-A-G

27877459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7136004-A-G

27877510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7136057-G-T

27877561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7136095-A-G

27877577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7136111-C-G

27877577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7136111-C-T

27877636-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7136168-G-C

27877636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7136168-G-T

27877904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7136458-T-G

27878474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7136982-G-A

http://identifiers.org/hco/10/GRCh38#27878550-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7137056-A-C

27878550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7137056-A-G

27878597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7137084-A-G

http://identifiers.org/hco/10/GRCh38#27878705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7137193-C-A

http://identifiers.org/hco/10/GRCh38#27878961-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7139365-A-C

27879001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7139405-A-G

27879002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7139406-T-A

27879460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7139817-A-G

27879461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7139818-T-C

27879633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7139947-A-T

27879650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7139964-G-A

http://identifiers.org/hco/10/GRCh38#27880113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7140394-C-A

27880232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7140512-T-C

27880294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7140560-T-C

27880381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7140642-C-T

27880387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7140648-G-T

27880480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7140757-A-G

27880581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7140849-G-A

27880585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7140853-T-A

27880675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7140923-T-C

27880918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7141121-G-A

27880933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7141135-C-G

http://identifiers.org/hco/10/GRCh38#27880936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7141138-C-A

27880936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7141138-C-T

27880938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7141140-T-C

27880971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7141161-G-A

27881112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7141262-G-A

27881267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7141461-C-T

27881858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7141727-T-A

27889488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7150641-G-A

27890645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7154144-G-A

27890645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7154144-G-T

27890689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7154182-G-C

27890712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7154205-G-A

27891005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7154524-A-G

27891366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7154884-C-T

27891452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7154974-C-T

27891623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7155131-T-C

27891625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7155132-C-T

27893504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 7155885-C-T

27893519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 7155870-G-T

27893521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 7155868-A-G

27896064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7156595-A-G

27896078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7156609-T-A

27896199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7156706-T-C

27896714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7157161-C-T

27896945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7157420-C-T

27897005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7157470-C-T

27897231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7157689-T-G

27897740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7158254-C-T

27897911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7158433-G-A

27897912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7158434-G-T

27897913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7158435-C-T

27907639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7181711-G-A

27907639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7181711-G-T

27907714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 7181785-G-A

http://identifiers.org/hco/10/GRCh38#27908250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7182295-C-A

http://identifiers.org/hco/10/GRCh38#27908387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7182431-C-A

27908595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7182639-G-A

27909044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7183122-T-C

27909083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7183173-T-A

27909865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7183647-T-A

27909865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7183647-T-C

http://identifiers.org/hco/10/GRCh38#27910006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7183767-C-A

27910227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7183950-A-G

http://identifiers.org/hco/10/GRCh38#27910322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7184048-C-A

27910336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7184062-C-T

http://identifiers.org/hco/10/GRCh38#27910357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7184083-C-A

27910357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7184083-C-T

27911920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 7185761-G-A

http://identifiers.org/hco/10/GRCh38#27912004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7185845-A-C

27912172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7186015-C-T

27912251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7186091-T-C

27912347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7186184-C-G

27912347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7186184-C-T

27912406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7186235-T-A

27912406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7186235-T-C

27912459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7186475-C-T

27912561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7186528-A-G

27912651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7186614-T-G

27914813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7190101-A-G

27914931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7190228-T-A

27914969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7190267-T-A

27914969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7190267-T-C

27914976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7190274-T-C

27915160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7190431-T-C

27915229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7190491-G-A

27915265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7190527-T-C

27915471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7190716-T-A

27915471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7190716-T-G

27915988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7191097-G-C

27916085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7191188-G-T

27916155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7191241-A-G

27916161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7191247-G-A

27919747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7198295-G-A

27919827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7198369-T-C

27919885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7198427-A-G

http://identifiers.org/hco/10/GRCh38#27920067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7198575-A-C

http://identifiers.org/hco/10/GRCh38#27920084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7198592-C-A

27920118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7198617-G-A

27920177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7198682-T-C

27920282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7198762-T-C

http://identifiers.org/hco/10/GRCh38#27920978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7199778-C-A

27921362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7199995-A-G

27921436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7200070-T-A

27921438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7200072-T-C

27921452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7200086-T-G

27921459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7200093-T-C

27921459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7200093-T-G

27921475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7200106-A-G

27921483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7200114-G-C

27921632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7200277-T-A

http://identifiers.org/hco/10/GRCh38#27921779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7200482-A-C

27927278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7205348-C-G

27927278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7205348-C-T

27927443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7205502-T-A

27927451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7205510-A-G

27927493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7205554-G-C

27927705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7205772-T-C

http://identifiers.org/hco/10/GRCh38#27927914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7206040-A-C

27928121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7206212-G-C

27928372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7206415-C-T

27931024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7208028-T-C

27931032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7208036-A-G

27931032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7208036-A-T

27931073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7208080-T-C

27931097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7208100-T-G

27931285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7208255-A-G

http://identifiers.org/hco/10/GRCh38#27934592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7211017-C-A

27934785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7211169-G-A

27934867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7211258-G-A

27934867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7211258-G-T

http://identifiers.org/hco/10/GRCh38#27934872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7211262-C-A

27935016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7211405-C-G

http://identifiers.org/hco/10/GRCh38#27935310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7211710-A-C

27935349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7211789-C-T

27935352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7211792-A-G

27935484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7211915-G-C

27935967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7213233-T-C

27936139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7213395-G-C

27936291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7213659-G-A

27936333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7213707-A-T

27936827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 7214670-C-T

27939277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7216250-T-C

27939893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 7216931-G-A

27939893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 7216931-G-T

27939915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 7216953-G-A

27939915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 7216953-G-C

27939915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 7216953-G-T

27940011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 7217049-G-A

27940011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 7217049-G-C

27940034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7217074-G-T

27940761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 7217946-T-C

27941145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7218700-C-G

27943268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7220707-G-A

http://identifiers.org/hco/10/GRCh38#27943486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7220971-C-A

27944029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7222328-G-T

27944120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7222452-C-G

27944120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7222452-C-T

27944513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7223245-T-C

http://identifiers.org/hco/10/GRCh38#27944515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7223247-C-A

27944515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7223247-C-T

http://identifiers.org/hco/10/GRCh38#27944716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7223458-C-A

27945033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7223750-G-A

27945033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7223750-G-T

27945092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7223815-T-A

27945092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7223815-T-G

27945321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7224042-G-T

27946947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7231738-C-T

27946966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7231757-A-G

27947446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7232032-C-G

27947543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7232110-G-C

http://identifiers.org/hco/10/GRCh38#27947549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7232116-A-C

http://identifiers.org/hco/10/GRCh38#27947719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7232234-C-A

27947719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7232234-C-T

27947797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7232290-G-C

27947961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7232445-C-T

27948938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7233914-T-C

27949372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7234351-G-A

27949383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7234362-T-C

27949596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7234574-C-T

27950026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7235149-A-G

27951065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7236029-G-C

27951079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7236042-T-C

27951611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7236632-A-T

27953377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7252492-C-T

27953385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7252500-T-C

27953684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7252787-A-G

http://identifiers.org/hco/10/GRCh38#27953685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7252788-A-C

27954342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7253458-C-T

27954559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7253914-T-C

27954618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7253972-G-A

27954648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7254002-C-T

27955697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7256494-G-T

27955707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7256504-G-A

27955878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7256624-C-G

27955878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7256624-C-T

27956016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7256757-T-A

27956196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7256890-C-G

27956218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 7256909-T-A

27957113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7257746-G-T

27957123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7257756-C-T

http://identifiers.org/hco/10/GRCh38#27957132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7257765-C-A

27957132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7257765-C-T

27957135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7257768-G-T

27957291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7257907-G-T

http://identifiers.org/hco/10/GRCh38#27957348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7257961-C-A

27957348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7257961-C-G

27957348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7257961-C-T

27957377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7257990-T-A

27957458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7258069-G-T

http://identifiers.org/hco/10/GRCh38#27957484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7258095-C-A

27957484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7258095-C-T

27957507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7258118-A-G

27957530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7258149-A-G

27957565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7258191-A-G

http://identifiers.org/hco/10/GRCh38#27957725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7258396-C-A

27957725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7258396-C-G

27957972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7258628-G-A

27957972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7258628-G-C

27958287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259105-T-C

27958307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259125-G-T

27958324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259142-T-C

27958690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259482-T-C

27958712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259504-T-C

27958712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259504-T-G

27958716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259508-C-G

27958734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259526-T-G

27958749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259541-T-C

27958749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259541-T-G

27958759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259551-A-T

27958772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259564-G-A

27958772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259564-G-T

27958814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259601-G-A

27958814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7259601-G-T

http://identifiers.org/hco/10/GRCh38#27958835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7259622-C-A

http://identifiers.org/hco/10/GRCh38#27958838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7259646-C-A

27958838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 7259646-C-T

27958928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7259717-C-G

27958936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7259725-A-G

27961607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7265040-T-C

http://identifiers.org/hco/10/GRCh38#27961679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7265112-A-C

27968897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7266858-A-G

27968929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7266889-A-G

http://identifiers.org/hco/10/GRCh38#27970478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7268133-A-C

27970478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7268133-A-G

27970532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7268188-G-C

27971180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7268472-T-C

27971270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7268547-A-G

27971389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7268665-T-A

27971389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7268665-T-C

http://identifiers.org/hco/10/GRCh38#27971416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7268688-C-A

27971498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7268773-C-T

27981046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7272849-T-A

27981220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7272999-C-G

27981220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7272999-C-T

http://identifiers.org/hco/10/GRCh38#27981234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7273016-A-C

http://identifiers.org/hco/10/GRCh38#27981607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7273298-C-A

27982069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7273783-T-C

27982569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7284228-G-T

27982573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7284232-T-C

27982573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7284232-T-G

27982576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7284235-T-C

27982635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7284298-G-A

27982668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7284331-T-C

27983062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7284692-C-T

27983178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7284753-G-A

27983316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7284864-G-A

27983316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 7284864-G-C

27983555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7285055-T-C

27983652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7285159-G-A

27983656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7285163-T-A

27983760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7285265-G-A

27983760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7285265-G-T

27983808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7285313-A-G

27983990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7285494-T-C

27984114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7285615-T-C

27984349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7285848-T-C

27984388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7285887-T-G

27984402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7285901-G-A

http://identifiers.org/hco/10/GRCh38#27984406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7285905-A-C

27984406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7285905-A-G

27984729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7286510-G-A

http://identifiers.org/hco/10/GRCh38#27985081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7286723-A-C

27985146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7286782-C-T

27985219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 7286852-A-G

27985219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 7286852-A-T

27985237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7286869-A-G

27985237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7286869-A-T

27985339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7286961-C-T

27985357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7286979-T-A

27985357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7286979-T-C

27986914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7288104-G-C

27986914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7288104-G-T

27986974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7288157-A-T

27987277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7288388-T-C

http://identifiers.org/hco/10/GRCh38#27987314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7288415-C-A

27987314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7288415-C-T

http://identifiers.org/hco/10/GRCh38#27987325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7288426-C-A

27987339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7288436-A-T

27987344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7288441-G-A

27987344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7288441-G-T

http://identifiers.org/hco/10/GRCh38#27987638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7288724-C-A

27987638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7288724-C-T

27987670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7288756-G-C

http://identifiers.org/hco/10/GRCh38#27987719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7288802-A-C

http://identifiers.org/hco/10/GRCh38#27987763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7288850-C-A

27988252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7289304-T-G

27988727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7289876-T-C

27988894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7290025-T-A

27988923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7290047-T-C

http://identifiers.org/hco/10/GRCh38#27989031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7290111-A-C

27989209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7290281-G-T

27989273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7290340-G-A

27989287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7290354-T-G

27989378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7290441-G-T

27989446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7290501-C-T

27989543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7290584-T-C

27992191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7292810-T-C

27992384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7293019-C-T

27993862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7293561-T-C

27994129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7293776-C-T

27994136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7293783-G-A

27994518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7294114-C-T

27994884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7294352-A-T

27994903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7294371-C-T

27995092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7294561-T-C

27995172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5 prime UTR variant
orthologous variants: 7294622-G-C

27995315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7294733-A-G

27995481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7294902-A-T

http://identifiers.org/hco/10/GRCh38#27995485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7294906-C-A

27995568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7295034-G-T

27995673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7295131-A-G

27995703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7295148-T-C

27995718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7295163-T-G

27995719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7295164-G-A

27995719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7295164-G-T

27995820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron variant
orthologous variants: 7295261-T-C

http://identifiers.org/hco/10/GRCh38#27996368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7295748-A-C

27996416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron variant
orthologous variants: 7295795-A-G

27997410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron variant
orthologous variants: 7296762-T-C

27997458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron variant
orthologous variants: 7296820-A-G

27997488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron variant
orthologous variants: 7296850-T-C

http://identifiers.org/hco/10/GRCh38#27999298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#7298158-A-C

27999647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25583
most severe consequence: 5 prime UTR variant
orthologous variants: 7298671-G-T