http://identifiers.org/hco/5/GRCh38#74721255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#97312960-C-A

74721255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97312960-C-G

74721255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97312960-C-T

74721262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97312953-T-A

74721262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97312953-T-G

http://identifiers.org/hco/5/GRCh38#74721321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#97312816-C-A

74721342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97312789-C-G

74721342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97312789-C-T

74721359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97312772-A-G

http://identifiers.org/hco/5/GRCh38#74721365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#97312766-C-A

74721394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97312737-G-A

74721394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97312737-G-T

74721654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97312235-T-C

74721654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 97312235-T-G

74721684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 97312205-G-A

74721834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97312055-T-G

74721898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97312006-G-A

74721898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97312006-G-T

http://identifiers.org/hco/5/GRCh38#74722194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#97311704-C-A

74722212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97311687-T-C

74722272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97311639-A-G

74722540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97311389-G-C

http://identifiers.org/hco/5/GRCh38#74722959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97311159-A-C

74723099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97311048-A-G

74725218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97310186-T-C

74725576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97309622-A-G

74725725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97309476-A-G

74725831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97309378-G-A

74725831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97309378-G-C

74725831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97309378-G-T

74725847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97309362-A-T

74725921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97309275-C-G

http://identifiers.org/hco/5/GRCh38#74725977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97309161-C-A

74726060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97309084-A-G

74726502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97308781-A-T

74726644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97308656-T-C

74729819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97308489-C-G

74729830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97308479-A-G

http://identifiers.org/hco/5/GRCh38#74729894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97308419-A-C

74730076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97308269-A-G

74730096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97308249-G-C

http://identifiers.org/hco/5/GRCh38#74730139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97308225-C-A

74730169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97308205-T-A

74730502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97307677-A-T

http://identifiers.org/hco/5/GRCh38#74730729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97307493-C-A

74730729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97307493-C-T

74730756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97307466-G-A

74730756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97307466-G-C

74730799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97307443-T-C

http://identifiers.org/hco/5/GRCh38#74730832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97307400-A-C

74730832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97307400-A-T

74730852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97307381-T-A

74730852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97307381-T-C

74730864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97307369-A-G

74731226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97305519-G-A

74731226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97305519-G-T

74732891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97304933-A-G

74733016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97304854-A-G

http://identifiers.org/hco/5/GRCh38#74733187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97304641-C-A

74733187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97304641-C-G

74733187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97304641-C-T

74733494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97304188-C-G

74733524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97304119-T-A

74733605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97304040-A-G

74733820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97303865-G-C

74733897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97303824-T-C

74733949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97303779-C-G

74733949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97303779-C-T

74734059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97303683-C-G

74735256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97302898-A-G

74735544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97302497-C-T

74735628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97302426-T-G

74735693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97302368-A-G

74736523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97302258-A-G

http://identifiers.org/hco/5/GRCh38#74736588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97301901-A-C

74736614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97301875-A-G

74736688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97301822-A-G

74736688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97301822-A-T

74736739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97301754-C-T

74736750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97301743-A-G

74736828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97301671-G-A

74736874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97301625-G-T

74736913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97301586-C-G

74737075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97301448-G-T

http://identifiers.org/hco/5/GRCh38#74737080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97301443-C-A

74737111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97301416-T-C

74737111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97301416-T-G

74737534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97300966-C-G

74737609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97300853-T-C

74737763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97300586-T-G

74737798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97300551-T-G

74737863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97300483-C-G

74737876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97300466-G-A

74737986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97300350-T-C

74738255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97299761-G-C

74738255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97299761-G-T

74738288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97299710-A-G

74738595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97299405-T-A

74738595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97299405-T-C

74738610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97299390-G-A

http://identifiers.org/hco/5/GRCh38#74738908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97299164-C-A

74738972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97299093-T-G

74739802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97297854-T-C

http://identifiers.org/hco/5/GRCh38#74739812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97297842-C-A

74739820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97297834-G-A

74739862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97297797-T-C

http://identifiers.org/hco/5/GRCh38#74739954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97297708-C-A

74739954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97297708-C-T

74739972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97297690-T-C

74739976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97297686-A-T

74739981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97297681-A-G

74740009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97297653-T-C

74740016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97297646-G-A

74740016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 97297646-G-T

74740121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97297541-T-C

http://identifiers.org/hco/5/GRCh38#74740246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97297413-C-A

74740246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97297413-C-T

http://identifiers.org/hco/5/GRCh38#74740248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97297411-C-A

74740248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97297411-C-T

74740264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97297393-G-A

74740264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97297393-G-C

74740264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97297393-G-T

74741289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97296899-C-T

74741325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97296864-A-G

74741447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97296754-A-T

http://identifiers.org/hco/5/GRCh38#74741509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97296691-C-A

74741509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97296691-C-T

74741532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97296670-T-C

74741630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97296575-G-A

74741630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97296575-G-T

74741698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97296531-A-T

74743378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97294461-G-A

74743646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97294215-T-C

74743646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97294215-T-G

74743657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97294204-T-C

74743838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97293598-C-T

74743930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97293515-A-G

http://identifiers.org/hco/5/GRCh38#74743989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97293457-A-C

74744523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97293149-C-T

74744643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97293043-T-C

74744669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97293018-T-C

http://identifiers.org/hco/5/GRCh38#74744686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97292959-A-C

74744922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97292683-G-A

74744989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97292609-T-C

http://identifiers.org/hco/5/GRCh38#74745586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97292160-C-A

74745706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97292078-G-A

74745792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97291992-A-G

74745917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97291884-G-A

74745917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97291884-G-T

74745961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97291874-A-G

74745961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97291874-A-T

74745962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97291873-T-C

74745968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97291867-T-C

74745968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97291867-T-G

74746033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97291820-G-A

74746033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97291820-G-T

74746062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97291796-A-G

74746081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97291777-A-G

74746151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97291710-A-G

http://identifiers.org/hco/5/GRCh38#74746166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97291695-C-A

74746166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 97291695-C-T

74746173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97291688-A-G

74746305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97291594-C-T

74746309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97291592-T-G

74746700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97291223-T-C

74746764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97290643-T-C

74747190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97290260-T-A

74747387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97290084-T-C

74747390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97290078-G-A

74747628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97289885-T-C

74747659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97289854-C-T

http://identifiers.org/hco/5/GRCh38#74747855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97289689-C-A

74747896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97289647-A-G

74747908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97289635-A-G

74748040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97289503-G-A

74748047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97289496-C-T

74748148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97289404-A-G

74750311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97287190-T-C

74750360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97287143-C-T

74750418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97287065-C-T

http://identifiers.org/hco/5/GRCh38#74750516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97286982-C-A

74750518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97286980-T-C

74750531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97286967-A-T

74750537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97286961-T-A

74750537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97286961-T-C

74750720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97286774-G-T

74750732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97286762-T-A

74750792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97286728-T-C

74751188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97286097-C-G

http://identifiers.org/hco/5/GRCh38#74751217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97286068-C-A

http://identifiers.org/hco/5/GRCh38#74751232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97286053-C-A

74751232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97286053-C-T

http://identifiers.org/hco/5/GRCh38#74751303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97285997-A-C

74751303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97285997-A-T

http://identifiers.org/hco/5/GRCh38#74751304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97285996-C-A

74751336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97285972-A-G

74751385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97285923-T-C

74751406-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97285902-T-A

http://identifiers.org/hco/5/GRCh38#74751448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97285860-C-A

74751448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97285860-C-T

74751499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97285809-C-G

74751509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97285799-A-G

http://identifiers.org/hco/5/GRCh38#74751592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97285719-A-C

74752067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97285301-C-T

http://identifiers.org/hco/5/GRCh38#74752325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

74758750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282911-T-A

74758750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282911-T-C

http://identifiers.org/hco/5/GRCh38#74758752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97282909-C-A

74758752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282909-C-T

74758780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282890-T-G

74758818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282852-G-A

74758818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282852-G-C

74758818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282852-G-T

http://identifiers.org/hco/5/GRCh38#74759007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97282663-C-A

74759063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282606-A-G

74759083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282505-G-A

74759083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282505-G-T

74759084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282504-T-A

74759351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282228-T-C

74759369-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 97282210-T-A

74759369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 97282210-T-C

74759437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282142-G-A

74759437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282142-G-T

74759444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282135-A-G

74759482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282096-T-C

http://identifiers.org/hco/5/GRCh38#74759511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97282067-A-C

74759518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97282060-T-C

http://identifiers.org/hco/5/GRCh38#74760122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97280416-C-A

74760306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97280176-C-T

74760678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97279824-C-G

74760679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97279823-T-G

74760730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97279773-T-C

74763308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97278929-A-G

74763696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97278500-G-C

74763696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97278500-G-T

74763751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 97278445-T-C

74763751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 97278445-T-G

74763785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97278409-A-G

74764194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97277686-T-C

74764244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97277636-T-C

http://identifiers.org/hco/5/GRCh38#74764245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97277635-C-A

74765264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97276063-A-G

74765394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97275958-C-G

74765394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97275958-C-T

74765424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97275930-A-T

74765516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97275865-G-A

74765778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97275602-C-T

74766576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97274961-A-T

74766768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97274788-G-T

http://identifiers.org/hco/5/GRCh38#74766792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#97274763-C-A

74766792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97274763-C-T

http://identifiers.org/hco/5/GRCh38#74766831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#97274731-C-A

74766863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97274702-T-C

74766948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97274618-G-A

74766948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 97274618-G-T

74766973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 97274586-C-T

http://identifiers.org/hco/5/GRCh38#74767029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97274547-A-C

74767029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 97274547-A-G

http://identifiers.org/hco/5/GRCh38#74767039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#97274541-C-A

74767039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 97274541-C-T

74767132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 97274490-G-A

74767132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 97274490-G-C

74767132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29682
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 97274490-G-T