http://identifiers.org/hco/3/GRCh38#196639790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31984277-C-A

196639790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31984277-C-T

196639821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31984249-G-A

196639821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31984249-G-T

196639908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31984167-G-A

196639908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31984167-G-T

196639963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31984115-A-G

196639963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31984115-A-T

196639966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31984105-T-C

196639971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31984100-G-A

196639971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31984100-G-T

196640616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31983480-C-T

196640721-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31983363-T-G

http://identifiers.org/hco/3/GRCh38#196641043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31983236-C-A

196643454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31982368-C-T

196643518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31982299-T-C

196643870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31982174-G-A

http://identifiers.org/hco/3/GRCh38#196643899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31982139-A-C

196643956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31982099-C-T

196644052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31982009-G-A

196645176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31980159-A-G

196645364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31979984-T-C

196645365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31979983-G-A

196645867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31979628-G-A

196646029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31979489-G-C

196646029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31979489-G-T

196646576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31979182-C-T

196646577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31979181-G-A

196646624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31979132-G-C

196649126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31976265-C-G

196649886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31975848-C-T

196649989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31975744-G-A

196649999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31975734-C-T

196651188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31975601-G-A

196652389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31974082-C-T

196652409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31974061-C-T

196652444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31974025-G-C

196652686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973723-C-T

196653442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973052-G-A

196653495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973001-G-A

196653495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31973001-G-C

196653580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31972910-G-A

196653597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31972893-C-T

196653600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31972890-G-C

196653606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31972884-A-G

196653667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31972828-G-A

196653755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31972730-G-A

196654025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 31972470-G-T

196654530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31966486-T-C

196654531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 31966485-G-A

http://identifiers.org/hco/3/GRCh38#196654657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31966358-C-A

196654657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31966358-C-T

196654673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31966342-G-A

196654731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31966280-T-A

http://identifiers.org/hco/3/GRCh38#196656302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31965839-C-A

196656579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31965438-G-A

196656659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31965350-G-A

http://identifiers.org/hco/3/GRCh38#196656721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31965280-C-A

196656725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31965276-C-T

196659806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31963767-C-T

196659842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31963731-A-G

196659921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31963652-T-G

http://identifiers.org/hco/3/GRCh38#196660092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31963481-C-A

196660092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31963481-C-T

196660190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31963383-C-T

196660328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31963245-C-T

196660403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31963170-A-G

http://identifiers.org/hco/3/GRCh38#196660967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31962606-C-A

196661027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31962546-G-A

196661096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31962477-A-G

196661096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31962477-A-T

196661378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31962195-T-C

196661642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31961928-T-C

196661645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31961925-A-T

196661708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31961862-T-G

196661741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31961833-C-T

http://identifiers.org/hco/3/GRCh38#196661769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31961807-C-A

196661769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31961807-C-T

196661795-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31961783-T-A

196661795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31961783-T-C

196661795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31961783-T-G

196661805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31961773-G-A

196661805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31961773-G-T

http://identifiers.org/hco/3/GRCh38#196661850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31961727-C-A

196662071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31961538-G-A

196662071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31961538-G-C

196662071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31961538-G-T

196662086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31961522-G-A

196662140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31961468-G-T

196662458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31961362-G-A

196662641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31961312-T-C

196662895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31961069-A-G

http://identifiers.org/hco/3/GRCh38#196662922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31961046-C-A

196662934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31961034-G-A

196662959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31961009-G-A

196663192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31960794-A-G

196663324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31960717-C-G

196663550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31960245-T-C

196663719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31960086-C-G

http://identifiers.org/hco/3/GRCh38#196664065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31959712-A-C

196664087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31959689-T-C

196667487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31950029-A-G

196667487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31950029-A-T

http://identifiers.org/hco/3/GRCh38#196667511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31950005-C-A

196667511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31950005-C-T

196667604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31949910-G-A

196667604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31949910-G-C

196667670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31949844-A-G

196667708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31949809-C-G

196667708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31949809-C-T

196667720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31949797-G-A

196670398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31949358-C-T

196670401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31949355-C-T

196670455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31949313-T-C

196670457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31949311-G-C

http://identifiers.org/hco/3/GRCh38#196670760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31949001-A-C

196671514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31948623-A-G

196671753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31948428-C-T

http://identifiers.org/hco/3/GRCh38#196671805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31948379-C-A

196671805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31948379-C-T

http://identifiers.org/hco/3/GRCh38#196671973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31948217-C-A

http://identifiers.org/hco/3/GRCh38#196677461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31944024-A-C

196677475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31944003-T-A

196677571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31943898-C-G

196677571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31943898-C-T

196677608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31943865-G-A

196677608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31943865-G-T

196677694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31943789-G-C

http://identifiers.org/hco/3/GRCh38#196677774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31943694-A-C

196677775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31943693-T-C

196677836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31943616-A-G

196677933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31943516-C-G

196678222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31943247-G-C

http://identifiers.org/hco/3/GRCh38#196678322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31943160-C-A

196681226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31936908-G-A

196681265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31936869-G-A

196681363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31936776-G-A

196681631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31936486-C-G

196681870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31936334-C-T

196681979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31936205-A-G

196681998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31936181-C-G

196682037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31936105-G-A

196682318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31935741-A-G

196682420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31935661-G-A

196684804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, undefined
orthologous variants: 31934494-T-C

http://identifiers.org/hco/3/GRCh38#196684833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31934462-A-C

196684974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, undefined
orthologous variants: 31934366-T-C

196685089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, undefined
orthologous variants: 31934283-T-C

196685099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, undefined
orthologous variants: 31934274-C-T

196685547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31934061-A-G

196686377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31933604-A-G

196688263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31932697-T-C

196688315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31932660-G-A

196688319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31932656-T-C

196688447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31932544-G-A

196688502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31932472-C-T

196688541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31932438-G-A

196689330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31931950-A-G

196694295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31929967-G-A

196694296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31929966-T-C

196706327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31926824-T-C

196706611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31926561-G-A

http://identifiers.org/hco/3/GRCh38#196706772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31926420-C-A

196706852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31926360-A-G

196706855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31926357-C-T

196706892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31926324-C-T

196707335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31926236-T-C

http://identifiers.org/hco/3/GRCh38#196707339-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31926232-A-C

196707339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31926232-A-G

196707461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31926146-A-T

196707711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31925923-T-C

196707744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31925890-T-A

196707744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31925890-T-C

http://identifiers.org/hco/3/GRCh38#196707939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31925707-C-A

196707939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31925707-C-T

196707952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31925694-C-G

196707952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31925694-C-T

196707966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31925680-G-A

196707966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31925680-G-T

196708497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31922894-A-T

http://identifiers.org/hco/3/GRCh38#196708509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31922882-A-C

196708570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31922821-G-A

196708570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, missense_variant
orthologous variants: 31922821-G-C

196708669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31922722-T-C

196708680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31922711-G-A

http://identifiers.org/hco/3/GRCh38#196708708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31922683-A-C

196708708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31922683-A-G

196708734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31922659-G-A

196708734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 31922659-G-T

http://identifiers.org/hco/3/GRCh38#196708789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31922610-C-A

196709718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31920095-T-G

http://identifiers.org/hco/3/GRCh38#196711052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31919433-C-A

196711131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31919349-T-A

196711623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31919185-T-C

196711691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31919092-C-G

196711800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, undefined
orthologous variants: 31919011-C-T

http://identifiers.org/hco/3/GRCh38#196711841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31918994-C-A

196711841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron variant
orthologous variants: 31918994-C-T

196711951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31918905-C-T

http://identifiers.org/hco/3/GRCh38#196712020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31918851-C-A

196712020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918851-C-G

http://identifiers.org/hco/3/GRCh38#196712028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31918843-C-A

196712028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918843-C-T

196712090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918782-A-G

196712122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918750-G-A

196712122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918750-G-T

196712146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31918716-G-A

196712156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31918706-G-A

196712169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918677-G-A

196712169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918677-G-C

196712169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918677-G-T

http://identifiers.org/hco/3/GRCh38#196712170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31918676-A-C

196712170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918676-A-G

http://identifiers.org/hco/3/GRCh38#196712171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31918675-C-A

196712171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918675-C-T

196712193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918655-G-C

196712193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918655-G-T

196712309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, undefined
orthologous variants: 31918569-A-G

196712375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, undefined
orthologous variants: 31918523-G-A

196712375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: intron_variant, undefined
orthologous variants: 31918523-G-T

196712397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31918500-A-G

196712397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31918500-A-T

196712429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918476-A-G

http://identifiers.org/hco/3/GRCh38#196712446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31918463-C-A

196712446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918463-C-T

196712455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918461-A-G

196712455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31918461-A-T

http://identifiers.org/hco/3/GRCh38#196712478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#31918439-C-A

196712478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31918439-C-T

http://identifiers.org/hco/3/GRCh38#196712507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#31918410-C-A

196712507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31918410-C-T

196712513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31918404-G-A

196712513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31918404-G-T

196712525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31918393-C-T

196712590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 31918346-A-G

196712590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 31918346-A-T

http://identifiers.org/hco/3/GRCh38#196712623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#31918313-A-C

196712623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 31918313-A-G

196712631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 31918305-G-A

196712631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 31918305-G-T

http://identifiers.org/hco/3/GRCh38#196712670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#31918270-C-A

196712670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31918270-C-T

196712681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31918258-A-G

196712681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 31918258-A-T

http://identifiers.org/hco/3/GRCh38#196712760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31918210-C-A

196712760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31918210-C-T

196712819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 31918151-G-A

196712819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 31918151-G-T

196712850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31918124-G-A

196712850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31918124-G-T

196712882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31918098-C-T

196712892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31918088-A-G

196712933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31918046-G-A

196712933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31918046-G-T

196712982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 31917995-G-T

196716275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31917193-T-C

196716276-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31917192-T-G

196716318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31917141-A-G

196716585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31916784-A-G

196716714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31916671-G-T

196716728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31916651-A-G

196716729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31916650-G-T

196716730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31916649-G-A

196716730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31916649-G-C

196716730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31916649-G-T

196716770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31915962-G-T

196716773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31915959-T-C

196716966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31915771-T-A

196716966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31915771-T-C

196722080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31911646-C-T

196722356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 31911363-A-G

196722599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31911119-G-T

196722606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31911112-G-A

196722682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31911033-G-A

196722682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31911033-G-T

http://identifiers.org/hco/3/GRCh38#196727775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31906473-A-C

196727823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31906442-G-T

196727840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31906425-G-A

196727840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31906425-G-T

196727843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31906422-T-C

http://identifiers.org/hco/3/GRCh38#196727846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31906418-A-C

196727846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31906418-A-G

196727846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31906418-A-T

196728001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 31906245-A-T

196730844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31904336-T-C

196730860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31904320-G-T

196730874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31904306-G-A

196730874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31904306-G-T

196730902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31904278-T-C

196730923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31904235-G-T

196730927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 31904231-A-T

http://identifiers.org/hco/3/GRCh38#196730980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31904178-C-A

196731100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 31904048-A-G

196731100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 31904048-A-T

http://identifiers.org/hco/3/GRCh38#196731124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#31904025-C-A

196733758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, splice_acceptor_variant
orthologous variants: 31903443-G-A

196733758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: NMD_transcript_variant, splice_acceptor_variant
orthologous variants: 31903443-G-T

196733906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 31903295-T-C

196733997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 31903220-G-A

196733997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 31903220-G-C

196734170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 31902975-A-G

196734231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 31902914-G-A

196734231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 31902914-G-T

196735504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26046
most severe consequence: 3 prime UTR variant
orthologous variants: 31902191-T-C