42095165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47785079-T-A

42099805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 47783767-C-T

42099807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 47783765-G-A

42099807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 47783765-G-T

http://identifiers.org/hco/6/GRCh38#42099825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#47783747-A-C

42099930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47783637-G-C

42100158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 47783415-G-A

42100318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47783300-A-G

42100368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 47783253-G-A

42100419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 47783206-G-A

42101585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47781511-G-T

42101734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47781365-G-T

42101756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47781346-G-C

42101756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47781346-G-T

42101759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47781343-C-T

42101797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47781317-C-T

42101853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47781263-T-C

42102020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47781126-A-G

42102031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47781121-C-T

http://identifiers.org/hco/6/GRCh38#42102198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47780987-C-A

42103048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780816-T-C

42103057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780813-G-A

42103057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780813-G-C

42103078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780792-G-A

42103180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780729-T-C

42103211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780712-T-C

42103250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780676-G-A

42103263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780666-G-A

42103263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780666-G-T

42103305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780651-G-A

42103305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780651-G-T

http://identifiers.org/hco/6/GRCh38#42103319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47780645-C-A

42103319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780645-C-T

42103368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780598-G-T

42103519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780542-T-C

42103519-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780542-T-G

http://identifiers.org/hco/6/GRCh38#42103520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47780541-C-A

42103520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780541-C-G

42103520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780541-C-T

http://identifiers.org/hco/6/GRCh38#42103521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47780540-C-A

42103521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780540-C-G

42103521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780540-C-T

42103533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780528-C-G

42103533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780528-C-T

http://identifiers.org/hco/6/GRCh38#42103536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47780525-C-A

42103536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780525-C-G

42103536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780525-C-T

42103628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780442-G-T

42103667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780402-A-G

http://identifiers.org/hco/6/GRCh38#42103686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47780384-C-A

42103686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780384-C-T

http://identifiers.org/hco/6/GRCh38#42103691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47780379-C-A

42103691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780379-C-G

42103691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47780379-C-T

42103843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 47780234-A-G

42103864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47780213-G-A

42103864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47780213-G-T

42103906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47780160-A-G

42104351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47779862-G-C

42104351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47779862-G-T

42104399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47779841-C-T

42104404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47779836-G-A

42104437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47779802-C-G

42104437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47779802-C-T

http://identifiers.org/hco/6/GRCh38#42104466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#47779773-C-A

42104466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 47779773-C-T

42104499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 47779713-C-T

42104557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 47779658-T-C

42104562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 47779653-G-A

42104562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 47779653-G-T

42104603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47779612-G-A

http://identifiers.org/hco/6/GRCh38#42104714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47779501-C-A

42104714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47779501-C-T

42104821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47779395-G-A

42104821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47779395-G-T

42104877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47779353-G-T

42105041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47779189-G-A

42105041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47779189-G-T

42105402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47778822-G-A

42105402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, stop_gained
orthologous variants: 47778822-G-T

42105523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47778701-G-A

42105523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47778701-G-T

42105527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47778697-T-C

42105799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47778461-G-A

42105883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47778284-A-T

42105887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47778280-G-A

http://identifiers.org/hco/6/GRCh38#42106028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47778139-A-C

42106101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47778066-C-T

42106125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47778042-T-C

42106128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47778039-A-G

42106403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47777767-G-C

42106403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47777767-G-T

42106430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47777740-T-C

42106550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47777620-C-G

42106550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47777620-C-T

42106599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47777571-G-C

42106599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47777571-G-T

42106671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47777499-G-A

42106671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47777499-G-T

42106824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47777346-G-T

42106874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47777296-G-T

42106968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47777202-A-T

42107004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47777166-T-G

42107043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47777127-G-T

42107073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47777097-G-A

http://identifiers.org/hco/6/GRCh38#42107079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47777091-C-A

42107184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47776986-T-G

42107231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47776939-T-A

42107231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47776939-T-G

42107361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47776827-G-A

42107361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47776827-G-T

42107373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47776815-G-A

42107373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47776815-G-T

http://identifiers.org/hco/6/GRCh38#42107385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47776803-A-C

42107385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47776803-A-G

42107385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47776803-A-T

42107412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47776773-G-A

42107412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47776773-G-C

42107412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47776773-G-T

http://identifiers.org/hco/6/GRCh38#42107511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47776674-C-A

42107520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47776665-C-G

http://identifiers.org/hco/6/GRCh38#42107562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47776623-C-A

42107562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 47776623-C-T

42107636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47776362-G-T

42107731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47776240-G-T

42109511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47775520-G-A

http://identifiers.org/hco/6/GRCh38#42109662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47775435-C-A

42109864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47775290-G-C

42109912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47775248-G-T

http://identifiers.org/hco/6/GRCh38#42109936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47775222-C-A

42109936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47775222-C-T

42109967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47775188-T-G

42110015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47775140-C-T

42110100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47775075-G-A

42110100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47775075-G-T

42110137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47775034-G-A

42110137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47775034-G-T

http://identifiers.org/hco/6/GRCh38#42110162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47775001-A-C

42110162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47775001-A-G

42110174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47774989-G-T

42110176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47774987-A-G

42110385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47774801-T-G

42111081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47773855-T-C

42114562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47771165-C-T

42114588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47771139-C-T

42114609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47771119-G-T

42114619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47771110-G-A

42114661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47771066-C-T

42114735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47770995-T-C

42118141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47766468-T-C

42118569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47765950-G-A

http://identifiers.org/hco/6/GRCh38#42118640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47765899-C-A

42118698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47765859-G-C

42120267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47765588-G-A

42120267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47765588-G-T

42120272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47765574-A-G

42120272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47765574-A-T

42120279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47765570-C-T

42120396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47765467-A-G

42120624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47765205-G-A

42120624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47765205-G-T

42121345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47764235-A-G

42121381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47764197-G-A

42121550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47764060-G-A

42121810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47763828-T-C

http://identifiers.org/hco/6/GRCh38#42121944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47763732-C-A

42121944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47763732-C-T

42122329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47762787-G-A

http://identifiers.org/hco/6/GRCh38#42122331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47762785-C-A

http://identifiers.org/hco/6/GRCh38#42122441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47762671-C-A

42122441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47762671-C-T

42122533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47762611-A-G

42122533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47762611-A-T

42122555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47762590-T-G

42122980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47762208-A-G

42124059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47761186-C-T

42124613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47760723-G-T

42124630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47760696-G-A

42124667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47760662-G-A

42124667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47760662-G-C

42124896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47760508-C-G

42124947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47760474-G-A

42125100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47760370-G-A

42125144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47760330-T-G

http://identifiers.org/hco/6/GRCh38#42125516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47760011-C-A

42125557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47759971-G-A

42125567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47759961-A-G

http://identifiers.org/hco/6/GRCh38#42128541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47757717-C-A

42128541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47757717-C-G

42128541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47757717-C-T

42128590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47757674-G-T

42128657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47757610-C-G

42128657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47757610-C-T

42128718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 47757548-A-G

42128852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47757428-T-C

http://identifiers.org/hco/6/GRCh38#42128883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47757398-C-A

42128883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47757398-C-G

42128883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47757398-C-T

42128894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47757395-G-A

42128894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47757395-G-T

42128896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47757393-G-A

42128896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47757393-G-T

42128932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47757363-C-T

42129121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47757187-G-T

42129298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47757004-G-C

42129307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47756995-C-T

42129453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47756846-G-A

42129476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47756820-T-C

42129555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47756743-G-C

42131752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47755884-G-C

42135064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47754608-C-T

http://identifiers.org/hco/6/GRCh38#42135067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47754605-C-A

42135085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47754587-A-G

42135113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47754558-C-T

42135232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47754438-G-A

42135354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47754319-G-C

42135496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47754164-C-T

42135765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47753870-C-T

http://identifiers.org/hco/6/GRCh38#42136833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#47752651-C-A

42137475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47751631-G-A

42137598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47751505-T-A

42137645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47751459-C-G

42139135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47750669-C-T

42139141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47750663-A-G

42139257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47750573-C-T

42139339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47750493-A-G

42139363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47750470-C-T

42139942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47749930-A-G

http://identifiers.org/hco/6/GRCh38#42140173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#47749725-C-A

42140173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47749725-C-G

42140311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47749605-C-T

42140419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47749519-T-C

42140496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47749451-G-A

http://identifiers.org/hco/6/GRCh38#42140604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47749360-C-A

42140810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47749169-T-C

42140810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47749169-T-G

42141123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47748851-C-G

42141154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47748820-G-A

42141154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47748820-G-C

42141329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47748726-C-T

42141684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47748418-G-A

42141784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47748288-A-G

42142179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47748019-T-C

42142179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47748019-T-G

42142285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47747887-C-T

http://identifiers.org/hco/6/GRCh38#42142490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47747681-C-A

42142490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47747681-C-T

42142501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47747670-G-A

42142501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47747670-G-T

42142599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47747568-G-A

42142599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21288
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 47747568-G-C