129904076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59308046-G-A

129904184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59308141-G-A

http://identifiers.org/hco/5/GRCh38#129904233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59308189-A-C

129904374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59308328-G-A

129904374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59308328-G-T

129904382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59308336-G-A

129904487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59308433-A-G

http://identifiers.org/hco/5/GRCh38#129904501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59308447-C-A

129904501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59308447-C-G

129904501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59308447-C-T

129904632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59308565-G-A

129904633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59308566-G-A

129904633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59308566-G-T

http://identifiers.org/hco/5/GRCh38#129904688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59308606-C-A

129904688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59308606-C-T

129904699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59308617-T-C

129904751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59308670-G-A

129904751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59308670-G-C

129904751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59308670-G-T

129904818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59308737-G-A

129904818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59308737-G-C

129904818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59308737-G-T

129904937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59308856-G-T

129905024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59308943-G-A

129905024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59308943-G-C

129905024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59308943-G-T

http://identifiers.org/hco/5/GRCh38#129905152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59309071-C-A

129905152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59309071-C-T

129905279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59309198-G-A

129905279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59309198-G-C

129905279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59309198-G-T

http://identifiers.org/hco/5/GRCh38#129905294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59309213-C-A

129905294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59309213-C-T

129905320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 59309239-C-T

129905510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59309435-G-A

129905606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59309531-C-G

129905606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59309531-C-T

http://identifiers.org/hco/5/GRCh38#129905674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59309598-A-C

129905674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59309598-A-T

129905780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59309705-T-A

129905780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59309705-T-C

129905780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59309705-T-G

129905828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59309753-G-C

129905828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59309753-G-T

129905870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59309795-T-A

129905870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59309795-T-C

http://identifiers.org/hco/5/GRCh38#129905959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59309877-C-A

129905959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59309877-C-T

http://identifiers.org/hco/5/GRCh38#129906005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59309918-C-A

129906005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59309918-C-T

129906028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59309945-G-A

129906028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59309945-G-T

129906120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59310038-G-A

129906304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59310201-C-T

129906343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, undefined
orthologous variants: 59310237-G-T

129906402-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59310294-T-G

129906536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59310423-G-T

129906627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59310518-C-T

129906677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59310569-G-T

http://identifiers.org/hco/5/GRCh38#129906759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#59310648-C-A

129906759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, undefined
orthologous variants: 59310648-C-T

http://identifiers.org/hco/5/GRCh38#129906802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59310690-C-A

129906908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59310773-T-C

129906909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59310774-A-G

129907477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59311365-C-T

129907590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59311493-A-G

129907642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59311544-A-G

129907645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59311547-C-T

129907955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59312213-C-T

129907990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59312251-A-G

129907990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59312251-A-T

129908061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59312321-G-A

129908061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron variant
orthologous variants: 59312321-G-T

129908262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59312522-G-A

129908327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59312587-T-C

129908357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 59312617-C-G

129908357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59312617-C-T

129908393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59312650-T-C

129908438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59312695-T-C

129908503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59312744-T-A

129908503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59312744-T-C

129908655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59312893-T-C

129908779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59312995-A-G

129908891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59313089-G-A

129908891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59313089-G-T

129908915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59313112-A-G

129909168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59313341-A-T

129909667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59313949-G-A

129912281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59314919-A-G

129912324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59314961-A-T

129912358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59314993-G-A

129912465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59315322-G-A

129913008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59315604-C-T

129913036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59315632-T-C

129913518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59317007-C-T

129913734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59317194-T-C

129914000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59317451-A-G

129914205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59317634-G-A

http://identifiers.org/hco/5/GRCh38#129914411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59317935-C-A

129914475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59317997-A-G

129914603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59318106-A-G

129914676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59318178-T-G

129914681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59318183-A-G

129914681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59318183-A-T

129915004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59318499-T-C

129915432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59318909-G-A

129915486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59318965-G-A

129915700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59319177-G-A

129915982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59319423-G-C

129916207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59319646-T-A

129916207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59319646-T-C

129916268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59319690-C-G

129916334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59319750-A-G

129916365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59319778-A-G

129916426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59319848-C-T

129916439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59319860-A-G

129916507-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59319929-T-G

http://identifiers.org/hco/5/GRCh38#129916759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59320109-A-C

129916759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59320109-A-G

129916793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59320141-A-G

129916855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59320200-T-A

129917125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59320436-T-C

129917423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59320594-G-A

http://identifiers.org/hco/5/GRCh38#129917712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59320861-A-C

129917737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59320886-A-G

http://identifiers.org/hco/5/GRCh38#129918212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59321669-A-C

129918332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59321790-C-T

129918388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59321852-G-A

129918388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59321852-G-T

129918609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59322084-A-G

129923775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59324056-G-A

http://identifiers.org/hco/5/GRCh38#129924197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59324544-A-C

129924197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59324544-A-G

129924216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59324582-C-T

http://identifiers.org/hco/5/GRCh38#129924331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59324691-A-C

129924362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59324747-T-C

129924373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59324758-C-T

129924390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59324784-G-A

129924390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59324784-G-C

http://identifiers.org/hco/5/GRCh38#129924760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59325208-A-C

129924815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59325243-C-T

129925037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59325478-G-A

129926598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59325759-G-C

http://identifiers.org/hco/5/GRCh38#129926627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59325787-C-A

129926627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59325787-C-T

129926815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59326376-C-T

129926833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59326389-T-A

129926853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59326411-T-A

129927022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59326579-A-T

129927042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59326617-A-G

129927339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59326884-T-C

129927345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59326890-A-G

129927463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59326995-C-T

http://identifiers.org/hco/5/GRCh38#129927538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59327044-A-C

129927539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327045-T-A

129927560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327065-T-C

129927572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327077-G-C

129927648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327142-T-C

129927649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327143-G-T

129927735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327234-T-C

129927894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327385-A-T

129928030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327528-T-A

129928311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327591-G-A

129928450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327714-T-G

129928593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327838-A-G

129928689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327931-G-T

http://identifiers.org/hco/5/GRCh38#129928701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59327943-C-A

129928701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327943-C-G

129928726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327969-G-C

129928738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327981-A-T

129928742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59327985-T-C

129928805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59328018-G-A

129928805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59328018-G-C

129928849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59328060-A-G

http://identifiers.org/hco/5/GRCh38#129929177-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59328387-A-C

129929329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59328555-A-G

129929374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59328593-C-T

129929762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59328940-T-G

129934596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59332456-T-A

129934604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59332464-T-C

129935084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59332727-A-G

129935591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59333572-G-T

http://identifiers.org/hco/5/GRCh38#129935662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59333643-C-A

129935799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59334107-A-G

129935889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59334196-A-G

129935919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59334226-G-A

129936582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59335138-G-C

129936646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59335208-G-A

129936674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59335233-A-T

129936816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59335351-G-T

129936854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59335389-G-T

http://identifiers.org/hco/5/GRCh38#129936932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59335467-A-C

129936932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59335467-A-T

129937010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59335532-T-C

129937028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59335550-T-C

129939750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59336153-G-A

129939762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59336165-T-C

129939986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59336373-T-C

129945061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59340856-G-A

129945061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59340856-G-T

129945117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59340911-T-C

129945184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59340971-G-T

129945330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59341129-C-G

129945411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59341206-A-G

129945558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59341345-T-G

129945653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59341442-G-T

129945736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59341518-A-G

129945761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59341537-G-A

129945771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59341548-A-G

129945771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59341548-A-T

129946263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59342121-A-G

129946357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59342201-G-C

129952684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59344591-A-G

129958201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59350046-G-C

129958942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59350738-G-A

129958942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59350738-G-T

129959130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59350920-G-A

129959157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59350958-G-A

129959747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59351761-A-G

129959951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59351952-T-C

http://identifiers.org/hco/5/GRCh38#129959993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59351991-C-A

129960475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59352982-T-G

129960669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59353161-G-A

129960921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59353418-T-C

129961341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59353821-T-G

129963032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59356937-G-A

129963284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59357160-G-T

129964145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59357861-G-C

129964345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59358006-T-A

129964470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59358107-A-G

129966110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59359256-C-T

129966236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59359382-A-G

http://identifiers.org/hco/5/GRCh38#129966240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59359386-A-C

129966295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59359440-C-G

129966455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59359574-G-A

129966455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59359574-G-T

129966540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59359652-A-G

129966710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59359816-G-T

129967669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59360806-G-A

129967760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59360897-C-G

http://identifiers.org/hco/5/GRCh38#129967804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59360941-A-C

129967994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59361128-C-G

129968216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59361311-T-C

129968267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59361361-T-A

129968605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59362414-G-C

129968642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59362457-T-C

129968676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59362490-G-A

129968749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59362556-C-T

129968851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59362658-T-C

129969027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59362815-T-C

129969309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59363072-T-C

129969415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59363179-A-G

129969651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59363416-A-G

129969888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59363630-A-G

129970048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59363801-C-T

129970110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59363859-T-C

http://identifiers.org/hco/5/GRCh38#129970216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59363969-C-A

129970268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59364012-A-G

129970849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59364490-T-C

129970901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59364544-A-G

129970909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59364552-A-G

129970927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59364570-C-G

129970927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59364570-C-T

129971008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59364627-A-G

129971226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59364839-T-G

129971353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59364929-G-A

129971449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59364997-A-G

129971545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59365086-C-T

129971626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59365164-T-A

129971626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59365164-T-C

129972124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59365615-G-A

129972443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59368500-T-C

129972518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59368566-C-T

129972632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59368650-C-G

129972748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59368737-G-T

http://identifiers.org/hco/5/GRCh38#129972947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59368901-C-A

129972947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59368901-C-G

129973250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59369197-G-T

129974131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59370266-A-G

129974147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59370282-A-G

129974182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59370318-C-T

129974252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59370384-A-G

129974271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59370403-A-G

129974293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59370425-C-G

129974336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59370468-T-C

129974397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59370529-A-G

129974824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59370925-A-T

129977463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59371684-G-A

129977463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59371684-G-C

129977594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59371797-T-C

129977617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59371820-A-G

129977617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59371820-A-T

http://identifiers.org/hco/5/GRCh38#129977841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59372026-C-A

129977844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372029-T-G

129977888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372063-T-A

129978036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372425-T-C

http://identifiers.org/hco/5/GRCh38#129978047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59372439-C-A

http://identifiers.org/hco/5/GRCh38#129978067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59372459-A-C

http://identifiers.org/hco/5/GRCh38#129978112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59372499-A-C

129978237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59372610-G-A

129982553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59375081-C-T

130017774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59379388-G-C

130017789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59379390-T-G

http://identifiers.org/hco/5/GRCh38#130017870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59379481-C-A

130018315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59379839-G-T

http://identifiers.org/hco/5/GRCh38#130018404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59379920-C-A

130018404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59379920-C-G

130018445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59379940-C-T

130018488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59379970-G-T

130019164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380167-T-C

http://identifiers.org/hco/5/GRCh38#130019424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59380371-A-C

130019478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380406-C-T

130019490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380418-A-T

130019715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380629-A-G

130019796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380710-C-T

130020097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59380999-T-C

130020109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381011-A-G

130020118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381020-G-A

http://identifiers.org/hco/5/GRCh38#130020487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59381044-C-A

130020487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381044-C-G

130020487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381044-C-T

130020498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381055-C-G

130020538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381095-G-A

130020538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381095-G-T

130020755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59381979-T-G

130020778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382009-T-A

130020779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382010-C-T

130021066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382623-A-G

130021424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59382960-A-T

130021608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383167-T-C

130021999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383611-T-G

130022070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383677-G-A

130022094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383701-C-G

130022198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59383803-T-G

130022446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59384164-T-C

130022617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59384338-A-T

130022733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59384452-T-C

130022759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59384478-C-T

130022834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59384583-T-C

130023544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59385243-A-G

130023873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59385564-C-T

130023924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59385673-C-T

130023979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59385782-A-G

130024097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59385982-T-A

130024110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59385994-T-C

130024129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386007-T-C

130024303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386174-T-G

130024381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386251-G-A

130024813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59386686-A-G

130025173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59387224-A-G

130025562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59388276-G-A

130025562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59388276-G-T

130025649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59388353-T-C

130025712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59388412-G-A

130025729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59388429-G-C

130026509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389132-A-T

130026638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389287-G-T

130026813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389455-C-T

130026981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389640-T-G

130026989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389648-T-A

130026990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389649-G-A

http://identifiers.org/hco/5/GRCh38#130031962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59389842-C-A

130032144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389982-A-T

130032159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59389997-G-A

130032666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59390476-A-G

130032666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59390476-A-T

130032843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59390593-G-A

130033210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59390906-T-C

130033253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59390954-G-A

130033302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391007-G-A

130033362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391080-G-A

130033465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391172-C-T

http://identifiers.org/hco/5/GRCh38#130033546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59391239-A-C

130033579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391273-C-G

130033587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391281-C-T

http://identifiers.org/hco/5/GRCh38#130033624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59391314-C-A

130033624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391314-C-T

130033704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59391458-T-G

130034123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394121-G-A

http://identifiers.org/hco/5/GRCh38#130034275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59394246-C-A

130034275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394246-C-T

http://identifiers.org/hco/5/GRCh38#130034287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59394258-A-C

130034334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394297-T-G

130034695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394655-G-C

130034857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394802-A-G

130034866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59394811-G-A

130035032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395009-G-A

130035033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395010-T-C

130035154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395111-G-T

130035232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395189-A-G

130035372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395321-A-G

130035377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395326-C-T

130035465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395417-G-A

130035500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395452-G-A

130035500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395452-G-C

130035924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395820-A-G

130035924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395820-A-T

130036052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395891-T-A

130036106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395942-G-C

130036125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395959-T-A

130036167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59395997-T-A

130036250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396085-C-G

130036411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396246-G-A

130036447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396279-A-G

130036570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396402-G-T

130036580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396412-A-G

http://identifiers.org/hco/5/GRCh38#130036593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59396425-C-A

130036593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396425-C-T

130036667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396489-G-A

130036692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396513-T-C

130036785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396608-G-A

http://identifiers.org/hco/5/GRCh38#130036885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59396714-A-C

130036971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396798-G-T

130037085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59396910-A-G

130037278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59397068-G-C

130037430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59397201-T-C

130037454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59397217-A-T

130037983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59397632-T-C

130037985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59397634-T-C

130038190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59397821-G-A

130040141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59404349-T-C

http://identifiers.org/hco/5/GRCh38#130040240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59404425-C-A

130040713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59404852-C-G

http://identifiers.org/hco/5/GRCh38#130040877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59405413-A-C

130040925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59405455-T-C

130041012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59405538-G-C

130041348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59405881-G-T

130042307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59406826-T-C

130043063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59407555-A-G

130043206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59407636-T-A

http://identifiers.org/hco/5/GRCh38#130043509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59407853-C-A

130043576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59407920-G-A

130043740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59411083-A-G

130043786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59411119-C-T

130044682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59413399-A-G

130045161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59413725-G-A

130045162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59413726-G-A

130045208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59413766-A-G

130045358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59413890-G-T

130045388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59413919-C-G

130045453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59413988-G-A

130045560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59414078-C-T

130046051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59414493-C-T

130046126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59414521-G-A

130046126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59414521-G-T

130046244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59414633-A-G

130046261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59414650-A-G

130046305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59414694-G-A

130046371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59414735-G-A

http://identifiers.org/hco/5/GRCh38#130046491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59414857-C-A

130046625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59414947-A-G

130046651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59414973-C-T

130051774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59415358-G-A

130051938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59415483-T-A

130051958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59415497-A-G

http://identifiers.org/hco/5/GRCh38#130051962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59415501-C-A

130051962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59415501-C-T

130052078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59415608-C-G

130052078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59415608-C-T

130055296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59417384-G-A

130055296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59417384-G-T

130055551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59417642-G-A

130055622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59417705-A-G

130055866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59418280-G-A

130055872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59418286-T-C

130056003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59418734-G-A

130056096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59418828-C-T

130056257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59418979-A-G

130056262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59418984-A-G

130056460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59419144-G-A

130056606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59419282-A-G

130057240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59419607-T-C

130057385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59419704-A-G

130057392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59419711-A-T

130057918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420352-G-A

130057918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420352-G-C

130057970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420402-A-T

130057992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420424-A-G

130058193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420615-A-T

130058330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420749-A-G

130058773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59420952-C-T

130059025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59421162-T-C

130059162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59421309-G-A

http://identifiers.org/hco/5/GRCh38#130059274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59421656-C-A

130059274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59421656-C-T

http://identifiers.org/hco/5/GRCh38#130059699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59422037-C-A

130059807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59422150-T-G

130063241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59423297-G-A

130063245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59423302-G-A

130063264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59423322-A-G

http://identifiers.org/hco/5/GRCh38#130063367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59423427-A-C

130063428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59423485-C-T

http://identifiers.org/hco/5/GRCh38#130063561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59423602-A-C

130063596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59423640-C-T

130063703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59423737-T-C

130063703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59423737-T-G

130063750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59423782-C-T

130063965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59423979-A-G

130063969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59423983-G-A

130064052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59424064-T-C

130064180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59424154-A-G

130064284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59424735-T-C

130064519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59424971-C-T

130064735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59425186-T-C

130064827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59425273-T-G

130065108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59426343-G-A

130065221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59426458-C-T

130065253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59426485-G-A

130065519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59426744-G-A

130065602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59426820-G-T

130065767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59426980-T-C

130066280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427483-A-G

130066294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427497-A-G

130066339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427542-C-G

130066570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427746-G-A

130066675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59427829-C-T

130066847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428006-G-A

130066926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428085-G-A

130066996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428154-T-G

130067042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428198-T-G

130067173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59428296-T-C

http://identifiers.org/hco/5/GRCh38#130067622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59433036-C-A

130067622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433036-C-T

130067771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433155-T-C

130067822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433205-G-A

130067829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433212-G-A

130067829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433212-G-C

130067855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433235-C-T

130067927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433283-G-A

130067927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433283-G-C

130068084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433430-C-T

130068097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433445-G-A

130068097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433445-G-T

130068367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433918-A-G

130068391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433942-G-T

130068406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59433956-G-A

130068454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59434004-A-G

130068573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59434100-G-A

130068573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59434100-G-T

http://identifiers.org/hco/5/GRCh38#130068769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59434290-C-A

130070461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59434612-C-T

130070680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59434828-A-G

130071362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59435954-C-T

130071690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59436202-T-A

130071788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59436286-T-G

http://identifiers.org/hco/5/GRCh38#130071824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59436322-C-A

130072103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59436589-C-T

http://identifiers.org/hco/5/GRCh38#130072307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59436811-C-A

http://identifiers.org/hco/5/GRCh38#130072426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59436891-C-A

130072538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437005-A-G

130072584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437107-A-G

130072844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437389-A-G

130072869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437405-T-A

130072869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437405-T-C

130072941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437472-G-A

130073037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59437567-A-G

http://identifiers.org/hco/5/GRCh38#130074457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59439834-A-C

130074548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439949-T-C

130074570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59439971-C-T

130074802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440257-G-T

130075030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440462-A-G

130075065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440501-C-T

130075105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440540-T-C

130075188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440607-C-G

130075320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440726-T-C

130075357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440758-G-C

130075357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440758-G-T

130075523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440914-T-C

130075562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440952-G-A

130075562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59440952-G-C

130075648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441140-A-G

130075770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441359-G-A

http://identifiers.org/hco/5/GRCh38#130075849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59441438-A-C

130075869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441458-C-T

130075890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441479-A-G

130076054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441632-T-C

http://identifiers.org/hco/5/GRCh38#130076105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59441664-A-C

130076117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441676-G-T

130076194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441751-A-G

130076339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441868-A-T

130076353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59441882-A-T

http://identifiers.org/hco/5/GRCh38#130076542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59442085-C-A

130076576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442116-T-G

130076589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442129-T-C

130076692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442235-G-A

130077504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442530-C-G

130077504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442530-C-T

130077553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442561-A-G

130077589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59442597-G-T

130077762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444604-T-C

130077854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444655-T-A

130077917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444727-C-T

130077965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444774-A-G

130078036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444840-A-G

130078038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444842-A-T

130078102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59444907-A-T

http://identifiers.org/hco/5/GRCh38#130078280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59445078-C-A

130078299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59445097-T-A

130078425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59445189-G-A

130078488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59445242-A-G

130078665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59445408-A-G

130078697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59445441-A-G

http://identifiers.org/hco/5/GRCh38#130078739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59445483-A-C

130078773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59445509-T-G

130078809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59445530-A-G

130078882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59445601-G-T

130079148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59445867-C-G

130079148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59445867-C-T

130079342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59446060-A-T

130079411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59446134-A-G

130079511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59446287-G-A

130079637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59446364-A-G

130079817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59446492-T-C

130080083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59446703-T-C

130080126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59446745-A-G

130080220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447002-G-A

130080515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447503-T-C

130080529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447518-G-C

http://identifiers.org/hco/5/GRCh38#130080578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59447566-A-C

130082149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447634-C-G

130082317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59447790-G-T

130083200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59448730-A-G

http://identifiers.org/hco/5/GRCh38#130083433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59449011-C-A

130083480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59449058-A-G

130083480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59449058-A-T

130083817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59449408-G-A

130084084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59449676-G-A

130084193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59449776-T-A

130084370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59449923-C-G

130084373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59449926-G-A

130084385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59449938-C-T

130085341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59450087-T-C

http://identifiers.org/hco/5/GRCh38#130085371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59450118-A-C

130089566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59450348-A-G

130089645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59450423-G-A

130089789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59450526-A-G

130089851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59450588-A-G

130089995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59450729-T-G

130090128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59451041-C-T

130090498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59451415-A-T

130090529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59451446-C-T

130090583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59451499-A-G

130090585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59451501-A-G

130090784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59451759-A-G

130090966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59451915-G-A

130091754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59452650-T-G

http://identifiers.org/hco/5/GRCh38#130091777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59452683-C-A

130091861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59452770-A-G

130091983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59452887-C-G

130092334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59453172-C-T

130092376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59453214-T-A

130092409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59453247-T-G

130092473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59453308-G-A

130093620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59454846-A-G

130093621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59454847-T-C

130093636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59454862-G-A

130093764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59454992-A-G

130093795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59455020-T-C

130093795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59455020-T-G

130093917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59455144-A-G

http://identifiers.org/hco/5/GRCh38#130094280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59456408-C-A

130094280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59456408-C-T

http://identifiers.org/hco/5/GRCh38#130094385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59456515-C-A

130098334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59456796-G-C

130098543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59456985-A-G

130098629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59457093-T-C

130099259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59457661-G-A

130099440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59457826-A-G

130099471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59457857-T-C

130099787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59458158-G-A

130099787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59458158-G-T

130099894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59458250-A-T

130101987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59458544-T-C

130102358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59458865-A-T

130102465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59458965-G-C

130102465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59458965-G-T

130102484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59458990-T-A

130102838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460106-T-C

130102900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460171-A-G

130102940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460206-G-A

130103305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460565-G-T

130103519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460768-G-A

130103519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460768-G-T

130103535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59460785-G-A

130103944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59461175-T-C

130104058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59461294-A-G

130104153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59461382-G-A

130104373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59461597-C-T

130104403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59461626-A-T

130104440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59461662-G-A

130105140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59462943-T-C

130105164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59462977-A-G

130105860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59463613-A-T

130105981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59463722-G-T

130106013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59463740-T-C

130106045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59463770-T-C

130106091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59463820-T-A

130106099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59463835-G-A

130106147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59463883-T-C

130106250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59463972-C-T

130106255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59463977-G-T

130106309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59465228-A-G

130106618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467544-G-C

130106723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467650-T-C

130106735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467662-T-A

130106735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467662-T-C

130106735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467662-T-G

130106798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467725-A-G

http://identifiers.org/hco/5/GRCh38#130106819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59467745-A-C

130106819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467745-A-G

130106828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59467754-T-C

130106925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59468307-A-G

130107196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59468572-G-A

130107209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59468583-A-G

130107272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59468643-A-G

130107593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59469167-T-C

http://identifiers.org/hco/5/GRCh38#130107795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59469365-A-C

130107795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59469365-A-T

130107801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59469377-C-T

130107872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59469432-A-G

130107972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59469536-G-A

130108778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59472001-G-T

130108859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59472072-C-T

130108943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59472152-T-C

130108957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59472166-C-T

130109216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59472387-C-T

http://identifiers.org/hco/5/GRCh38#130109316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59472467-A-C

130109653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59472774-C-T

130109961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59473076-G-T

130109977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59473089-C-T

130110079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59473188-G-A

130110390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59473963-T-A

130110505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59474064-A-G

http://identifiers.org/hco/5/GRCh38#130110508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59474067-C-A

130110600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59474158-T-C

130110697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59474256-G-A

130110817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59474435-G-C

130110995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59474566-C-T

130111014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59474587-G-A

130111152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59474726-A-G

130111152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59474726-A-T

130111497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59475117-C-T

130111552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59475165-A-G

130111631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59475225-T-A

http://identifiers.org/hco/5/GRCh38#130111763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59475347-A-C

130111763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59475347-A-G

130112394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59475757-A-G

130113174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59476454-T-G

130113248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59476521-A-G

130113260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59476533-C-T

130113575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59476832-C-T

http://identifiers.org/hco/5/GRCh38#130113623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59476886-C-A

130113629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59476892-T-C

130114122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59477550-A-G

130114129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59477589-T-A

130114145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59477635-T-C

130114145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59477635-T-G

130114269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59477757-T-C

130114277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59477765-A-G

130114328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59477815-G-A

http://identifiers.org/hco/5/GRCh38#130114351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59477838-C-A

http://identifiers.org/hco/5/GRCh38#130114587-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59477972-A-C

130114595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59477980-T-A

130114599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59477984-T-C

130114814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59478190-G-A

130114948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59478940-C-T

130115206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59479445-T-C

130115266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59479510-G-A

130115459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59479695-A-G

130115459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59479695-A-T

130115532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59479714-T-G

130115570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59479757-G-A

130115570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59479757-G-C

130115596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59479780-A-G

130115765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59479954-A-G

130115889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59480073-G-C

130115931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59480118-C-G

130115998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59480191-G-T

http://identifiers.org/hco/5/GRCh38#130116097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59480246-C-A

130116262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59480393-A-G

130116399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59480509-A-G

130116539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59480646-C-T

130116561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59480667-T-G

130117089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59481164-G-A

130117124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59481199-G-A

130117124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59481199-G-C

130117146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59481219-G-A

130117146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59481219-G-C

130117159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59481232-C-T

130117237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59481315-A-G

130117413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59481449-T-G

130117441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59481467-A-T

130117456-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59481481-C-G

130117637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59481641-A-G

130117783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59481764-A-T

130118682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59482112-T-G

130118802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59482188-A-G

130118924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59482302-C-T

130119079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59482441-G-A

130119116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59482479-G-A

130119116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59482479-G-T

130119137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59482491-C-G

130120914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59483698-G-C

130120994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59483772-C-T

http://identifiers.org/hco/5/GRCh38#130121185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59483929-A-C

130121231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59483975-G-A

130121306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59484050-A-T

130121743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59484500-G-T

130122135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59484988-A-G

http://identifiers.org/hco/5/GRCh38#130122159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59485016-A-C

130122198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59485104-A-G

130122201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59485107-T-C

130122378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59485275-G-C

130122520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59485401-C-T

130122522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59485403-G-A

130123123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59486090-C-T

130124068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59486397-G-A

130124068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59486397-G-T

130124082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59486409-G-A

130124082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59486409-G-T

http://identifiers.org/hco/5/GRCh38#130124111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59486438-C-A

130124111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59486438-C-T

130125514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59486900-C-T

130125633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59487021-G-A

130125798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59487191-T-A

130125981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59487382-A-G

http://identifiers.org/hco/5/GRCh38#130126139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59487541-C-A

130126317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59487714-G-A

130126317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59487714-G-C

130126348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59487743-C-T

130126532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59487918-G-A

130126532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59487918-G-T

130126700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59488054-C-T

130127051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59488353-A-G

130127080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59488378-T-C

130127173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59488987-G-A

130127173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59488987-G-C

130127173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59488987-G-T

130127199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59489010-T-G

130127293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59489114-C-T

130127369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59489187-C-T

130127420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59489237-T-C

130127434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59489251-T-C

130127510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59489331-C-G

130127510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59489331-C-T

130127739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59489537-G-A

130127742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59489540-T-C

130127751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59489546-G-A

130128032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59489820-A-G

130128074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59489860-A-G

130128175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59489959-A-T

130128652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59490317-T-C

130128679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59490344-A-G

130128848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59490524-A-G

130129878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59491794-G-A

http://identifiers.org/hco/5/GRCh38#130129944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59491952-A-C

130130175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59492160-G-A

130130217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59492224-T-C

130130217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59492224-T-G

http://identifiers.org/hco/5/GRCh38#130130290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59492301-C-A

130130518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59492481-C-T

130130817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59492793-C-G

130130988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59492959-C-G

130131070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59493028-T-C

130131100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59493058-A-G

130135612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59494629-C-G

130136266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59495285-G-A

130136451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59495459-G-A

130136466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59495474-C-T

130136640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59495645-C-T

130136689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59497204-A-G

130136791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59497321-G-T

130137113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59497795-A-G

130137140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59497819-G-A

130137282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59497944-C-T

130137392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59498045-T-A

130137470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59498117-T-G

130137501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59498156-T-C

130137535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59498191-G-T

130137549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59498209-T-C

130137622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59498348-T-C

130137657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59498385-A-G

http://identifiers.org/hco/5/GRCh38#130137880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59498599-A-C

130137908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59498626-T-C

130137970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59498776-A-G

130138195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59499018-G-C

130138347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59499166-G-A

130138694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59499505-C-T

130138765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

130139252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59503402-C-T

130139260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59503410-A-G

130139260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59503410-A-T

130139285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59503435-C-T

130139304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59503455-G-A

130139418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59503565-T-A

130139447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59503596-A-G

130139447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59503596-A-T

130139536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59503709-G-C

http://identifiers.org/hco/5/GRCh38#130139563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59503736-C-A

130139563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59503736-C-T

130139644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59503838-C-T

130142319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 59504456-T-C

130142540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59504649-A-G

130142824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59506455-G-T

130142880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59506512-C-G

130143103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59507068-A-G

130143137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59507101-G-T

130143368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59507344-A-G

130143406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59507376-G-A

130143406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59507376-G-T

130147152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59507767-A-T

130150632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59509453-A-T

130150872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59509717-G-A

http://identifiers.org/hco/5/GRCh38#130151398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59510249-A-C

http://identifiers.org/hco/5/GRCh38#130152026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59510488-C-A

130152138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59510603-T-C

130152189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59512282-C-T

130152561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59512633-G-C

130152764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59512810-T-C

130152856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59512901-C-G

130152883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59512941-G-T

130152946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59513005-G-T

130154915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59514692-T-C

130155190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59514955-G-A

130155190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59514955-G-C

130155200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59514965-T-G

130155250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59515015-A-G

130155795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59515538-T-C

130155876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59515622-G-C

130155899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59515647-T-A

130155985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59515755-G-A

http://identifiers.org/hco/5/GRCh38#130156121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59515891-C-A

130156257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59516016-A-T

130156336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59516093-T-C

130156388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59516145-C-T

130156972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59516735-G-C

130157253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59517010-A-G

130158315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59517385-C-T

130158578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59517591-C-T

130158659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59517661-G-A

130159550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59517891-T-G

http://identifiers.org/hco/5/GRCh38#130159689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59518023-C-A

130159777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59518125-G-C

130159920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59518206-A-G

http://identifiers.org/hco/5/GRCh38#130160271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59518484-C-A

130160551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59518755-C-T

130160562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59518765-G-A

http://identifiers.org/hco/5/GRCh38#130160595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59518798-A-C

http://identifiers.org/hco/5/GRCh38#130160640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59518857-C-A

130160643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59518860-A-G

http://identifiers.org/hco/5/GRCh38#130160685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59518902-C-A

130160748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59518972-C-G

130160748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59518972-C-T

130160798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59519021-G-A

130160832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59519055-G-A

130160839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59519062-C-T

130162423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59522866-A-G

130162757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59523023-G-A

http://identifiers.org/hco/5/GRCh38#130162859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59523119-A-C

130162872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59523133-G-A

130162872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59523133-G-T

130163123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59523353-T-C

http://identifiers.org/hco/5/GRCh38#130163416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59523794-C-A

130163444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59523825-A-G

130163642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59524006-C-G

130163646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59524010-A-G

http://identifiers.org/hco/5/GRCh38#130163704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59524049-A-C

130163731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59524071-T-C

130164108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59524553-C-T

130164346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59524784-G-A

130165532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59526501-G-A

130165600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59526571-C-T

130165733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59526707-A-G

130165784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59526753-T-G

130165874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59526847-A-G

130165952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59526891-G-C

130166307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59527432-T-G

130166357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59527483-G-A

130166457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59527577-C-T

130166485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59527606-T-C

130166580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59527709-C-T

130166883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59528005-G-A

130166889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59528010-A-G

http://identifiers.org/hco/5/GRCh38#130166913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59528034-C-A

130166928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59528049-C-T

130166949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59528070-C-T

130172654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59528788-C-G

130172682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59528818-T-G

130172691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59528827-A-G

130172691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59528827-A-T

130172828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59528963-T-C

130172836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59528971-A-G

130172909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59529096-A-G

130173032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59529197-T-G

130173179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59529339-G-A

130173214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59529374-G-T

130173338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59529469-G-T

130173551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59530079-G-C

130173615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59530143-T-A

130173987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59530481-A-G

130174024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59530521-A-G

130174467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59530992-A-G

130174556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59531071-A-T

http://identifiers.org/hco/5/GRCh38#130174565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59531080-C-A

130174664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59531169-A-G

130174681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59531170-A-T

130174767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59531250-A-G

130174795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59531272-A-G

http://identifiers.org/hco/5/GRCh38#130174821-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59531298-A-C

http://identifiers.org/hco/5/GRCh38#130174923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59531394-C-A

http://identifiers.org/hco/5/GRCh38#130177489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59536071-C-A

130177637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59536184-G-T

130177710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59536256-G-A

130177710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59536256-G-T

130177754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59536295-G-T

130177755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59536296-A-G

130177755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59536296-A-T

130177807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59536348-G-T

http://identifiers.org/hco/5/GRCh38#130177815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59536356-C-A

130177849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59536383-G-C

http://identifiers.org/hco/5/GRCh38#130177897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59536432-C-A

130177897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59536432-C-G

130177949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59536512-T-C

130177958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59536521-G-T

130178221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59536663-T-A

130178231-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59536673-A-T

130178236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59536678-T-C

130178316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59536700-C-T

130178760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59537975-G-T

130178968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59538157-A-G

130178983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59538172-A-G

130178994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59538187-C-T

130179162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59538320-A-G

130179450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59538585-G-A

http://identifiers.org/hco/5/GRCh38#130179470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59538597-C-A

130179470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59538597-C-T

130179474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59538601-C-T

130179555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59538838-C-T

130179686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59539040-G-A

130179715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59539076-T-C

130180153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59539515-C-T

130180175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59539537-C-T

130180202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59539564-T-A

130183078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59540846-G-A

130183158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59540921-G-A

130183252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59541049-C-T

http://identifiers.org/hco/5/GRCh38#130183396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59541207-C-A

130183396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59541207-C-G

130183677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59541514-C-G

130183803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59541602-G-C

http://identifiers.org/hco/5/GRCh38#130183817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59541616-A-C

130183817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59541616-A-T

130183838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59541635-C-T

130184042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59541797-C-T

130184077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59541829-A-G

130184077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59541829-A-T

http://identifiers.org/hco/5/GRCh38#130184123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59541875-C-A

130184123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59541875-C-T

http://identifiers.org/hco/5/GRCh38#130184174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#59541911-C-A

130184174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59541911-C-T

130184395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59542122-G-A

130184395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59542122-G-C

130184395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59542122-G-T

130184552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 59542279-A-G

130184825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 59542552-C-T

130184880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 59542607-G-A

130184909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 59542636-T-C

130185033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 59542760-T-C

130185122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 59542849-T-C

http://identifiers.org/hco/5/GRCh38#130185185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3_prime_UTR_variant, stop_gained
orthologous variants: http://identifiers.org/mco/18/GRCm39#59542912-C-A

130185185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 59542912-C-T

130185371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 59543098-T-C

130185515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 59543242-A-G

130186028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3 prime UTR variant
orthologous variants: 59543784-T-G

130186047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3 prime UTR variant
orthologous variants: 59543803-T-C

130186387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3 prime UTR variant
orthologous variants: 59544147-G-C

130186387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24293
most severe consequence: 3 prime UTR variant
orthologous variants: 59544147-G-T