http://identifiers.org/hco/21/GRCh38#34513225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92184592-A-C

34513240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non coding transcript exon variant
orthologous variants: 92184607-T-C

34513261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non coding transcript exon variant
orthologous variants: 92184631-G-A

34513289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 92184672-C-T

34513313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non coding transcript exon variant
orthologous variants: 92184704-T-A

34513320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non coding transcript exon variant
orthologous variants: 92184711-G-A

34513327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non coding transcript exon variant
orthologous variants: 92184718-T-A

34513389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92184775-T-C

34513398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92184784-T-C

34513426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92184806-C-T

34513428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92184808-G-T

34513489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92184861-G-T

34514249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92186281-T-C

34514281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92186329-C-G

34514281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92186329-C-T

34514282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92186330-G-A

34514309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92186362-C-T

34514384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92186446-C-T

http://identifiers.org/hco/21/GRCh38#34514525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92186535-A-C

34514602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92186605-T-C

34514719-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92186711-T-A

34514988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92186930-T-A

34514988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92186930-T-C

34515327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92187240-G-A

34516238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92188681-A-G

http://identifiers.org/hco/21/GRCh38#34516594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92188947-C-A

34516594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92188947-C-T

34516598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92188954-G-A

http://identifiers.org/hco/21/GRCh38#34516631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92188987-C-A

34516941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92189254-G-T

34516951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92189264-C-T

34517292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92189588-T-G

34517327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92189622-G-T

34517371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92189668-G-A

34517394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92189691-T-C

http://identifiers.org/hco/21/GRCh38#34517944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92190201-C-A

34517944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92190201-C-T

34517988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92190245-G-A

34517988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92190245-G-T

34517992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92190249-G-A

34517992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92190249-G-C

34517992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92190249-G-T

34518011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92190265-T-C

34518011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92190265-T-G

34518013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92190267-A-T

34518231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 92190491-C-T

http://identifiers.org/hco/21/GRCh38#34518317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92190570-C-A

http://identifiers.org/hco/21/GRCh38#34518322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92190575-A-C

34518322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92190575-A-G

34518323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92190576-A-G

34518335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92190583-G-A

34518335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92190583-G-T

34518342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92190590-T-G

http://identifiers.org/hco/21/GRCh38#34518540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92190723-C-A

34518540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92190723-C-T

34518887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92191198-C-T

34518895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92191206-T-C

34519024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92191335-A-T

34519090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92191391-C-G

34520320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92192085-C-T

34520343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92192108-T-C

34520378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92192130-G-C

34520383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92192135-T-G

34520399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92192150-C-T

34520401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92192152-C-G

34520401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92192152-C-T

34520582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92192321-A-G

34521182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92192487-G-T

http://identifiers.org/hco/21/GRCh38#34521239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92192538-C-A

34521239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92192538-C-T

34521264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92192558-G-A

34521264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92192558-G-T

http://identifiers.org/hco/21/GRCh38#34521347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92192628-A-C

34521347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 92192628-A-G

34521389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 92192667-T-C

34521486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92192741-G-A

34521486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92192741-G-C

34521486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92192741-G-T

34521590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92192845-G-A

34521617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92192872-T-C

http://identifiers.org/hco/21/GRCh38#34521693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92192946-C-A

34521693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92192946-C-T

34521707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92192951-C-T

http://identifiers.org/hco/21/GRCh38#34521718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92192962-C-A

34521718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92192962-C-T

34521720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92192964-G-A

34521720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92192964-G-T

34521778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92193033-T-A

34521778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92193033-T-G

34521811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92193063-T-A

34521811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92193063-T-C

34521811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92193063-T-G

34521840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92193089-G-A

34521840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92193089-G-C

34521840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92193089-G-T

34521842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 92193091-T-C

34522771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92193586-C-T

34522772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92193587-T-C

34522836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92193631-T-C

34522928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92193688-A-G

34522941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92193700-C-G

34522999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92193743-C-T

http://identifiers.org/hco/21/GRCh38#34523029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92193747-C-A

34523041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92193759-T-C

34523405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92194060-A-G

34523405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92194060-A-T

34523513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92194128-T-A

34523513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92194128-T-C

34523591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92194205-G-A

34523684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92194298-C-G

34523684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92194298-C-T

http://identifiers.org/hco/21/GRCh38#34523687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92194301-C-A

34524263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92194614-T-A

34524282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92194628-G-A

http://identifiers.org/hco/21/GRCh38#34524344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92194692-C-A

34524344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92194692-C-T

http://identifiers.org/hco/21/GRCh38#34524349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92194697-C-A

34524349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92194697-C-T

http://identifiers.org/hco/21/GRCh38#34524377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92194725-C-A

34524659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92194951-G-T

34524794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92195088-C-T

http://identifiers.org/hco/21/GRCh38#34524816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92195122-C-A

34524816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92195122-C-G

34524816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92195122-C-T

34524846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92195171-C-T

34524919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92195210-G-A

34524979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92195265-T-C

34524984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92195270-A-T

34525003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92195287-G-T

34525019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92195301-G-A

34525107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 92195375-G-T

34525131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 92195404-G-A

34525132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 92195405-A-G

34525141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 92195414-G-C

34525339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 92195608-T-A

34525387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 92195652-C-T

http://identifiers.org/hco/21/GRCh38#34525521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92195779-A-C

34525542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92195800-T-C

34525615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92195872-A-G

34525676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92195924-T-A

34525676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92195924-T-C

34525707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92195955-A-T

34526152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92196348-A-G

34526283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92196471-A-T

34526420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92196567-G-A

34526464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92196594-T-C

34526730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 92196851-T-C

34526850-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92196991-T-A

34526850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92196991-T-C

http://identifiers.org/hco/21/GRCh38#34526855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92196999-C-A

34526857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92197001-G-T

http://identifiers.org/hco/21/GRCh38#34526877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92197015-C-A

34526877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92197015-C-T

34526963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92197101-A-T

34527062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92197198-G-T

http://identifiers.org/hco/21/GRCh38#34527081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92197219-C-A

34527081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92197219-C-G

34527095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92197232-T-C

34527443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92197564-C-T

34528067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92198017-T-C

34528410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92198368-C-T

34528454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92198412-C-G

34536453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92199448-G-A

34536453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92199448-G-C

34536555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92199552-G-A

34536555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92199552-G-T

34536601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92199597-T-C

34536601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92199597-T-G

34536617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92199626-G-A

34536714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92199697-G-A

34536955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92200024-T-C

34537517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92200540-G-A

http://identifiers.org/hco/21/GRCh38#34537717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92200630-C-A

34537717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92200630-C-T

34537724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92200637-G-A

34537791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92200679-A-G

34537896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92200778-G-T

34538510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202439-C-T

34538757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202623-G-A

34538891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202725-C-T

34539008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202836-T-G

34539194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202983-G-A

34539197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92202992-C-T

http://identifiers.org/hco/21/GRCh38#34539210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92203016-C-A

34539210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92203016-C-G

34539210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92203016-C-T

34540212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92204933-T-C

34540497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92205565-G-A

34540511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92205579-C-T

34540633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92205699-C-G

34540679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92205745-G-C

34540679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92205745-G-T

http://identifiers.org/hco/21/GRCh38#34541297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92206393-A-C

34544817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92209056-C-T

34544818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92209057-G-A

34544944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92209164-G-A

34545396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92210031-T-C

34545528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92210109-G-C

34545548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92210122-G-C

34545548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92210122-G-T

34545559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92210133-C-T

34545773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92210351-C-T

34545834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92210402-C-T

http://identifiers.org/hco/21/GRCh38#34546402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92212409-C-A

34546402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212409-C-T

34546422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212425-G-A

34546428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212431-G-T

http://identifiers.org/hco/21/GRCh38#34546474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92212480-A-C

34546489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212491-T-A

34546583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212582-G-A

34546657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212652-T-C

34546697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212692-C-T

34546913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212895-G-C

34546913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92212895-G-T

34549331-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92216335-T-G

34549336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92216340-C-G

34549457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92216455-T-C

34549631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92216636-C-T

34549659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92216664-C-T

34549714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92216710-C-T

34549972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92216944-T-C

34550083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92217100-C-T

http://identifiers.org/hco/21/GRCh38#34550211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92217291-C-A

34550211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92217291-C-T

34550398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92217540-T-C

34550405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92217547-A-G

34550444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92217584-T-G

http://identifiers.org/hco/21/GRCh38#34550582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92217720-A-C

34550778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92217909-C-T

34550883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92217995-C-T

34550922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92218031-T-A

http://identifiers.org/hco/21/GRCh38#34551131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92218166-A-C

34551267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92218287-T-G

34551641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92218580-T-C

34551770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92218720-G-C

34551803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92218749-C-G

34551804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92218750-T-C

34551957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92218981-C-T

34552016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92219025-T-C

34552253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92219253-G-T

http://identifiers.org/hco/21/GRCh38#34552276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92219276-C-A

34552331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92219296-C-T

34552561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92219495-G-C

34552877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92219978-G-A

34553150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92220192-G-A

34553317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92220363-C-T

34553899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92220891-C-T

34554257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92221304-A-T

34557429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92223119-A-G

34557616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92223269-C-T

34557824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92223433-A-T

http://identifiers.org/hco/21/GRCh38#34557924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92223566-C-A

34558183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92223832-C-T

34558226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92223866-C-T

34558228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92223868-A-G

34558539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92224648-C-T

34558588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92224700-T-C

34558716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92224816-C-G

34558870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92224961-G-A

34559023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92225068-T-C

34559069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92225115-C-T

34559082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92225128-G-T

http://identifiers.org/hco/21/GRCh38#34559102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92225148-C-A

34559425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92225444-G-A

34559430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92225455-C-T

34559676-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92225683-T-G

34559700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92225706-T-C

34560418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92227388-C-T

34560455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92227425-A-T

34560748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92227700-G-A

34561545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92228068-T-A

34561633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92228360-C-G

34562074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92228881-C-G

34562260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92229042-T-A

34562260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92229042-T-C

34562278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92229059-C-T

34567747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92231800-C-G

34567797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92231849-C-T

34567853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92231885-C-T

34568086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92232035-G-A

34568086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92232035-G-C

34568248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92232172-A-G

http://identifiers.org/hco/21/GRCh38#34568310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92232218-C-A

34568474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92232344-T-C

34568505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92232361-G-A

34568557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92232395-A-G

34570233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92234057-A-G

34570365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92234475-T-A

34570564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92234634-G-T

34570763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92234822-A-G

34570861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92234920-A-G

34570874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92234933-T-A

34570874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92234933-T-C

34571463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92235215-T-C

34571968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92235428-G-A

34571991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92235449-A-G

34572108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92235852-A-G

http://identifiers.org/hco/21/GRCh38#34572202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92235943-A-C

34572255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92236001-C-T

34572595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92236290-T-A

34572595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92236290-T-G

34572612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92236312-A-G

34572623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92236323-C-T

34572670-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92236345-T-G

34573503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92237005-T-G

34573693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92237171-T-A

34573921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92237486-T-C

34573961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92237529-G-A

34574092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92237674-C-T

34574615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92238207-T-A

34574658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92238238-A-G

http://identifiers.org/hco/21/GRCh38#34576291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92238497-C-A

34579120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92239592-C-T

34579771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92240201-T-A

http://identifiers.org/hco/21/GRCh38#34579808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92240238-C-A

34580005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92240399-G-A

34580038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92240436-G-A

34580086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92240487-C-T

34580306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92240676-C-T

34580500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92240854-C-G

34580500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92240854-C-T

34580791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92241099-G-T

34581009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92241295-C-G

34581009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92241295-C-T

34582313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92242025-T-A

34582313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92242025-T-C

34583516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92243324-T-A

34583650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92243435-C-T

34583786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92243692-T-C

34583794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92243700-G-A

34583972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92243889-G-A

34584079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92243989-C-T

34584087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92243997-T-A

34584087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92243997-T-C

34584123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92244033-C-T

34584519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92244324-T-C

34584522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92244327-T-C

34584742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92244607-C-T

34584794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92244652-A-G

34589866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92245707-C-T

34589867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92245708-T-G

34589952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92245775-T-C

34590041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92245863-A-T

34590101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92245938-C-G

34590101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92245938-C-T

34590183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92246003-T-A

34590369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92246128-T-C

http://identifiers.org/hco/21/GRCh38#34590654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92246346-C-A

http://identifiers.org/hco/21/GRCh38#34590708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92246399-C-A

http://identifiers.org/hco/21/GRCh38#34593199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92246948-C-A

34593670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92247295-C-T

34593809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92247417-G-A

34593828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92247434-A-T

http://identifiers.org/hco/21/GRCh38#34593922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92247515-C-A

34593922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92247515-C-G

34593922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92247515-C-T

34594068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92247660-T-C

34594098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92247690-G-C

http://identifiers.org/hco/21/GRCh38#34594119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92247710-A-C

34594276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92247834-G-A

34594296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92247842-G-A

34594298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92247844-A-T

34594349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92247870-T-C

34594800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92248329-C-T

http://identifiers.org/hco/21/GRCh38#34594819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92248347-C-A

34594819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92248347-C-T

34595510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92248753-A-G

http://identifiers.org/hco/21/GRCh38#34595666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92248899-C-A

http://identifiers.org/hco/21/GRCh38#34595871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92249119-C-A

34596318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92249502-T-C

34596423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92249540-T-C

34596803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92249925-G-A

http://identifiers.org/hco/21/GRCh38#34596874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92250005-C-A

34596874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92250005-C-T

34596923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92250041-G-A

34596947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92250058-G-C

34597285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92250287-T-C

34597394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92250369-G-A

34597481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92250438-T-C

34597506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92250468-T-C

34597642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92250598-C-T

34603050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92252431-G-T

34603061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92252446-A-T

34603168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92252530-A-T

34603514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92252711-C-T

34603915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92253063-G-A

34604575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92253571-C-T

34606767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92254710-G-C

34606876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92254796-T-A

34606904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92254825-C-T

34607126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92255071-A-G

34609372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92257241-T-A

34609409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92257273-A-G

34609587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92257439-C-T

34610144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92257926-C-G

34610144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92257926-C-T

34611274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92259312-T-A

34611812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92259816-G-C

34612054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92260049-G-C

34612204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92260188-A-G

34612470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92260421-C-T

http://identifiers.org/hco/21/GRCh38#34612556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92260480-C-A

34612578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92260502-T-G

34612707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92260588-A-G

34612809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92260673-G-A

34612819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92260683-T-G

34613709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92261774-G-A

34613709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92261774-G-T

34613756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92261733-A-G

http://identifiers.org/hco/21/GRCh38#34613931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92262612-C-A

34613931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92262612-C-T

http://identifiers.org/hco/21/GRCh38#34614146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92262412-C-A

34614146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92262412-C-T

34614185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92262387-A-T

34614322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92262251-G-A

34614444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92262141-G-T

34614729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92262696-G-A

34614729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92262696-G-T

34614934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92262898-G-A

34614934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92262898-G-C

34614934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92262898-G-T

http://identifiers.org/hco/21/GRCh38#34614937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92262901-C-A

34614937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92262901-C-T

http://identifiers.org/hco/21/GRCh38#34614946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#92262910-C-A

34614946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92262910-C-G

34614946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92262910-C-T

http://identifiers.org/hco/21/GRCh38#34615021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#92262975-C-A

34615021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 92262975-C-T

http://identifiers.org/hco/21/GRCh38#34615029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3040
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#92262983-C-A