http://identifiers.org/hco/18/GRCh38#62187342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#105591672-C-A

62187342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105591672-C-T

http://identifiers.org/hco/18/GRCh38#62187351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#105591681-C-A

62187351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105591681-C-G

62187351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105591681-C-T

http://identifiers.org/hco/18/GRCh38#62187355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#105591685-C-A

62187408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105591733-G-A

62187424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105591749-T-C

62187428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105591753-T-C

62187476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105591803-G-A

62187476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105591803-G-C

62187476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105591803-G-T

http://identifiers.org/hco/18/GRCh38#62187634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#105591961-C-A

62187634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 105591961-C-T

62187667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105591994-G-A

62187667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105591994-G-T

62187729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105592056-C-T

62187747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105592074-C-T

62187750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105592077-T-C

62187750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105592077-T-G

62187883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105592210-G-A

62187883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105592210-G-T

http://identifiers.org/hco/18/GRCh38#62187934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105592261-C-A

62187934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105592261-C-G

62187934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105592261-C-T

62187944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105592271-A-T

62187974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105592301-G-T

http://identifiers.org/hco/18/GRCh38#62188054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105592381-A-C

62188054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592381-A-G

62188096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592422-G-A

62188096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592422-G-T

http://identifiers.org/hco/18/GRCh38#62188165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105592490-C-A

62188165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592490-C-T

62188181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592506-G-A

62188181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592506-G-T

http://identifiers.org/hco/18/GRCh38#62188320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105592639-C-A

62188473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105592782-G-A

http://identifiers.org/hco/18/GRCh38#62188474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105592783-C-A

62188915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105593217-A-G

62189061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105593334-G-A

62189061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105593334-G-C

62198515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105595029-G-A

62198515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105595029-G-T

62198611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105595129-C-G

62198750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105597704-T-C

62200249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105598525-T-C

62200330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105598598-G-C

62200468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105598724-G-C

62200585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105598794-G-A

62200585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105598794-G-T

http://identifiers.org/hco/18/GRCh38#62201515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105600008-A-C

62201554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105600038-A-G

62201625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105600109-A-T

62202345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601115-A-T

62202349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601119-G-C

62202356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601123-G-A

62202485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601483-C-T

62210955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605689-G-A

62211001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105605734-A-G

62211244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 105605979-T-G

62211953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105606348-G-A

62211981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105606376-C-T

62212059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105606442-C-T

62212064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105606447-A-G

62212070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105606451-G-A

62212070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105606451-G-C

http://identifiers.org/hco/18/GRCh38#62212085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105606462-C-A

62212089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105606474-A-G

62212113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105606498-G-A

62212115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105606500-G-T

62212280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105606657-T-C

62217263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105611585-A-G

62217527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105611897-G-T

62217718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105612070-C-T

62217885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105612229-C-T

62219415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105613157-G-T

62219898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105613606-A-G

62220066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105613811-T-C

62220167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105613900-T-G

http://identifiers.org/hco/18/GRCh38#62220741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105614399-C-A

62220741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105614399-C-T

62221298-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105614928-A-T

62221340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105614962-A-G

62221514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615133-T-C

62221736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615339-C-T

62221775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615378-C-T

http://identifiers.org/hco/18/GRCh38#62221798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105615408-A-C

62221798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615408-A-G

62222275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105616295-G-A

62222524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105616690-C-T

http://identifiers.org/hco/18/GRCh38#62225963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105618253-C-A

62225972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105618257-T-C

62226241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105618526-A-G

62226393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105618670-G-A

62226492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105618766-A-G

62227234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105619547-A-G

62227408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105619750-T-A

62227757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105620095-A-G

62227830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105620161-A-G

62228234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105620537-T-C

62228605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105620909-A-G

http://identifiers.org/hco/18/GRCh38#62228634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105620938-C-A

62228722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105621017-G-A

62228832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105621114-A-G

62229180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105621463-T-C

62229637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105621986-A-G

62229645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105621994-A-G

62229698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105622042-G-C

62229732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105622083-C-T

62229798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105622136-G-A

62229798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105622136-G-T

http://identifiers.org/hco/18/GRCh38#62229820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105622158-A-C

62230588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105622598-T-C

62231083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623020-G-T

62231138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623082-T-G

62231179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623123-T-C

62231188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105623147-T-C

62232223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105624129-G-T

62232291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105624193-G-A

62232291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105624193-G-T

62232362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105624256-G-A

62232362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105624256-G-T

62232465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105624359-A-G

http://identifiers.org/hco/18/GRCh38#62232546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105624428-C-A

http://identifiers.org/hco/18/GRCh38#62232915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105624776-A-C

62233043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105624899-G-T

62233351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105625094-C-T

62233539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105625285-G-C

62233539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105625285-G-T

62233587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105625328-A-G

62233858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105625585-G-A

62233858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105625585-G-C

62233988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105625730-T-G

62234430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105626078-A-G

62234751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105626360-G-A

62234774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105626383-G-C

62235267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105626759-G-T

62242328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105629541-G-A

62243344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630191-C-T

62243477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630322-G-A

62243575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630411-T-A

62243575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630411-T-G

62243740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630572-A-G

62243895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630674-T-G

62243900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630679-G-A

62243936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630699-A-G

62244188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630933-T-G

62244501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631439-G-A

62244575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631512-C-T

62244885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631777-G-A

62244885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631777-G-T

62244908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631802-A-G

62244945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631840-G-T

62244963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631858-A-G

http://identifiers.org/hco/18/GRCh38#62245013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105631905-C-A

62245217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105632064-G-C

62245676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105632196-T-A

http://identifiers.org/hco/18/GRCh38#62245935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105632369-C-A

62245935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105632369-C-T

62245962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105632400-T-G

http://identifiers.org/hco/18/GRCh38#62245963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105632401-C-A

62245963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105632401-C-T

http://identifiers.org/hco/18/GRCh38#62246006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#105632443-C-A

http://identifiers.org/hco/18/GRCh38#62246086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105632482-C-A

62246086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105632482-C-T

62246114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105632510-T-A

62246126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105632522-C-T

62246201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105632565-A-G

62247491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105636834-A-G

62247509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105636852-C-T

62249271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105638791-A-T

62249276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105638798-A-G

http://identifiers.org/hco/18/GRCh38#62249408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105638924-C-A

62249408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105638924-C-T

62250132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105639492-T-A

62250296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105639782-T-C

62250417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105640006-T-C

62250487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105640080-T-A

62250530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105640117-C-G

62250545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105640132-A-T

62250580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105640167-G-A

62252834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105641728-G-A

62252946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105641837-A-G

62253539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105642300-G-A

62253796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105642529-T-C

62254186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105643283-G-A

62254228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105643395-G-A

http://identifiers.org/hco/18/GRCh38#62254306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105643471-C-A

62254306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105643471-C-T

62254424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105643550-A-G

62254460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105643588-C-T

http://identifiers.org/hco/18/GRCh38#62254654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105643781-C-A

http://identifiers.org/hco/18/GRCh38#62254655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105643782-C-A

62254732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105643859-G-T

http://identifiers.org/hco/18/GRCh38#62254931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105644045-A-C

62255277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105644371-G-A

62255327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105644421-T-A

62255363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105644456-G-A

62255363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105644456-G-T

62255400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105644496-G-C

62255400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105644496-G-T

62255487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105644583-G-A

62255487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105644583-G-C

62255487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105644583-G-T

62255494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105644590-T-C

62255494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105644590-T-G

62256213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105645233-G-A

62256269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105645296-G-C

62257966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105646518-T-G

62258098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105646650-T-C

62258233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105646803-T-C

http://identifiers.org/hco/18/GRCh38#62258771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105647436-C-A

62258771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105647436-C-T

62258946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105647564-C-G

62259084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105647708-A-G

62261643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105649125-G-A

62261643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105649125-G-T

62261808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105649278-A-G

62261819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105649293-G-A

62261819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105649293-G-C

62262184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105649795-G-A

62262213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105649824-G-A

62263958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105653343-A-G

62263978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105653363-T-C

http://identifiers.org/hco/18/GRCh38#62264074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105653459-A-C

62264174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105653574-A-T

62264280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105653686-G-T

http://identifiers.org/hco/18/GRCh38#62264340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105653746-A-C

62264352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105653757-G-A

62264405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105653808-T-C

62264408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105653811-T-C

62264481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105653882-A-G

http://identifiers.org/hco/18/GRCh38#62264582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105653945-C-A

62264582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105653945-C-T

http://identifiers.org/hco/18/GRCh38#62264586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105653949-C-A

62264586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105653949-C-T

62264641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105653984-T-G

62264657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105653999-G-A

62264657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105653999-G-C

62264657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105653999-G-T

62264910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105654247-T-A

62265130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105654399-G-A

62265130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105654399-G-C

62265744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105654917-G-C

62266112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655193-G-A

62266288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655325-C-G

62266372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655426-C-T

62266569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655580-G-A

62266569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655580-G-C

62266569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655580-G-T

http://identifiers.org/hco/18/GRCh38#62266696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105655660-C-A

62266696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105655660-C-T

62266781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655744-A-G

62266782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655745-T-C

62266863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655833-G-A

62266863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655833-G-T

62267107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105656059-A-G

62267749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105656994-A-G

62267819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105657061-T-A

62267819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105657061-T-C

62268423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105658186-C-G

62268567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105658318-G-T

http://identifiers.org/hco/18/GRCh38#62268853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105658910-A-C

62268853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105658910-A-G

62268853-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105658910-A-T

62268964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105659024-T-C

62268964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105659024-T-G

62268966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105659026-A-G

62268966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105659026-A-T

62269267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105659298-G-T

62272857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105661091-A-G

62273242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105661627-G-A

62273252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105661637-T-C

62273385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105661725-G-C

http://identifiers.org/hco/18/GRCh38#62273974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105662237-C-A

62274105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105662369-T-A

62274105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105662369-T-C

http://identifiers.org/hco/18/GRCh38#62274120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105662397-C-A

62274120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105662397-C-G

62274223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105662646-T-G

62274392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105662873-C-T

62274500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105662972-A-T

62274564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105663023-G-A

62274613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105663068-T-C

http://identifiers.org/hco/18/GRCh38#62275083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105663385-A-C

62275222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105663488-T-C

http://identifiers.org/hco/18/GRCh38#62275317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105663596-C-A

62275317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105663596-C-T

62275362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105663636-T-C

62275477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105663751-T-A

62275477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105663751-T-C

62275498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105663771-G-A

62275498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 105663771-G-T

62275592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105663855-T-A

62275592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105663855-T-C

62275768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105664017-C-T

62276222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105664383-C-T

62276320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105664482-A-G

62276912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105665581-G-A

62276913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105665582-A-G

62276929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105665598-A-G

62277219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105665800-G-A

62277219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105665800-G-C

62277489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105665912-A-G

62277540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105665963-A-G

http://identifiers.org/hco/18/GRCh38#62277543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105665966-C-A

62277615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_lost
orthologous variants: 105666000-G-C

62277875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105666257-A-G

62277875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105666257-A-T

http://identifiers.org/hco/18/GRCh38#62277921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105666302-A-C

62277921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105666302-A-G

http://identifiers.org/hco/18/GRCh38#62277934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105666319-C-A

62277934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105666319-C-T

62277944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105666329-A-G

62278036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105666427-T-C

62278050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105666441-A-T

http://identifiers.org/hco/18/GRCh38#62278182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105666573-C-A

62278399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105666760-C-T

62279083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105667300-A-G

62279250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105667465-G-A

62279250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105667465-G-C

62279250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105667465-G-T

62279356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105667566-G-A

http://identifiers.org/hco/18/GRCh38#62279632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105668022-C-A

http://identifiers.org/hco/18/GRCh38#62279962-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105668339-A-C

http://identifiers.org/hco/18/GRCh38#62280249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105668627-A-C

62280249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105668627-A-G

62280796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105669173-T-C

http://identifiers.org/hco/18/GRCh38#62280799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105669176-C-A

62280799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105669176-C-T

62280856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105669218-A-G

62281154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105669399-T-G

62281312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105669517-A-G

http://identifiers.org/hco/18/GRCh38#62281446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105669635-A-C

62281624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105670121-T-C

62282160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105670760-A-T

http://identifiers.org/hco/18/GRCh38#62282168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105670804-C-A

62282168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105670804-C-T

62282181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105670817-G-T

62282187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105670823-G-A

62282187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105670823-G-T

62282223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105670855-T-C

http://identifiers.org/hco/18/GRCh38#62282257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105670903-C-A

62282257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105670903-C-T

62282478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105671099-G-A

http://identifiers.org/hco/18/GRCh38#62282558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105671172-C-A

62282558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105671172-C-T

62283494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105671661-G-A

62283512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105671683-C-T

62283595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105671764-G-C

62283712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105671873-G-A

62283730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105671890-G-C

62283879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105672029-A-G

62284083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105672131-A-G

62284168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105672216-T-G

62284495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105672465-T-C

62284511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105672487-T-C

62284511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105672487-T-G

http://identifiers.org/hco/18/GRCh38#62287445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105673888-C-A

62287571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105674019-A-G

62287571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105674019-A-T

62287943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105674301-G-A

62287988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105674333-G-A

62288574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105674912-A-G

62288615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105674961-G-A

62288633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105674979-A-G

62288708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105675055-A-G

62288708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105675055-A-T

62289251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105675549-G-A

62289413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105675674-G-T

http://identifiers.org/hco/18/GRCh38#62289433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105675690-A-C

62289436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105675693-A-G

62289616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105675923-T-G

62289781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676083-C-T

62290058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676308-A-T

http://identifiers.org/hco/18/GRCh38#62290634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105676716-A-C

62290634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676716-A-G

62290865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677147-C-T

http://identifiers.org/hco/18/GRCh38#62290909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105677190-C-A

62290909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677190-C-T

62290918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677199-G-A

62291069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677316-A-G

62291124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677374-G-A

62291124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677374-G-C

62291391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677871-A-T

http://identifiers.org/hco/18/GRCh38#62291422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105677899-A-C

62291422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677899-A-G

62291422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677899-A-T

62291444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677920-T-A

62291444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677920-T-C

62291456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677931-G-A

62291456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677931-G-C

62291456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105677931-G-T

http://identifiers.org/hco/18/GRCh38#62291532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105678037-C-A

62291532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105678037-C-T

http://identifiers.org/hco/18/GRCh38#62291544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105678048-C-A

62291574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105678078-T-C

http://identifiers.org/hco/18/GRCh38#62291738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105678251-C-A

62291738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105678251-C-G

http://identifiers.org/hco/18/GRCh38#62291750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105678263-C-A

62298932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105678831-G-A

62298967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105678861-T-C

62304504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105679972-G-T

62304604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105680074-A-G

62304813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105680281-G-A

http://identifiers.org/hco/18/GRCh38#62305283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105681014-C-A

62305283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105681014-C-T

http://identifiers.org/hco/18/GRCh38#62305553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105681366-C-A

62305553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105681366-C-G

62305553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105681366-C-T

62305684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105681494-T-A

62305684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105681494-T-C

62305746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105681556-A-G

62306070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105681907-G-A

62306070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105681907-G-T

http://identifiers.org/hco/18/GRCh38#62306580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105682398-C-A

http://identifiers.org/hco/18/GRCh38#62306599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#105682417-A-C

62306621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105682447-A-G

62306683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105682502-T-C

62306713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105682517-G-T

62306847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29289
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105682610-G-A