34254626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012903-G-C

34254685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012846-G-T

34254751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012795-G-A

34254751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012795-G-T

34255057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012563-G-C

http://identifiers.org/hco/19/GRCh38#34255061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#34012559-A-C

34255089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012531-C-T

34255091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012529-G-A

34255206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34012455-G-A

34256758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34011544-T-C

34257352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34010974-T-C

34259536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34009095-T-A

34259536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34009095-T-C

34260821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34008814-C-T

34260914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34008721-T-A

34260914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34008721-T-C

34260982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34008653-C-G

http://identifiers.org/hco/19/GRCh38#34261307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#34008426-C-A

34261307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34008426-C-G

34265126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34005661-T-A

34265233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34005570-G-A

34265533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34005296-C-T

34266132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34004744-A-G

34266684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34004324-A-G

34266727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34004277-T-C

34266741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34004260-A-G

34269770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34001887-T-C

34270065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34001612-T-C

34270084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34001593-G-A

34270248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34001434-A-G

34270880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34000172-C-T

34273642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33999109-G-A

34273705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33999068-C-G

34273705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33999068-C-T

34273829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33998977-T-C

34274833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33998744-T-A

34274833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33998744-T-G

34274849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33998728-G-A

34275192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33998372-G-A

34275192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33998372-G-T

34276438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33996284-A-G

34276439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33996283-G-A

34276651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33996094-T-C

34276694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33995916-C-T

http://identifiers.org/hco/19/GRCh38#34276710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33995900-C-A

34276710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33995900-C-G

34276764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33995850-G-A

34276764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33995850-G-C

34276967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33995648-G-T

34277191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33995448-C-G

34277308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33995340-T-C

34277308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33995340-T-G

34277309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33995339-A-G

34282685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33991058-A-G

http://identifiers.org/hco/19/GRCh38#34282691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33991055-C-A

34282691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33991055-C-T

34283002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33990750-C-G

34299585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33985481-T-C

34300285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33984814-A-G

34300380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33984717-G-A

34300380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33984717-G-T

34300646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33984447-C-G

34300646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33984447-C-T

34300669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33984424-G-A

34300669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33984424-G-C

34300669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33984424-G-T

34300755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 33984338-T-C

34300780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33984313-A-G

34300780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33984313-A-T

34300824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 33984269-C-G

34300824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 33984269-C-T

34301025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33984079-G-C

http://identifiers.org/hco/19/GRCh38#34301615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33983717-A-C

34303072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33983501-T-G

34305342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33981362-A-G

34305538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33981167-C-G

34305585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33981124-T-C

34307185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33977397-G-A

34307272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33977312-G-A

34307377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33977201-C-T

34307399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33977179-C-G

34307399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33977179-C-T

34308077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33976989-C-T

34308276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33976669-G-A

34308276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33976669-G-T

http://identifiers.org/hco/19/GRCh38#34309086-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33973769-A-C

34309245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33973618-A-G

34309780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33972896-T-C

34309952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33972718-A-G

34310177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33972591-A-G

34310313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33972479-C-T

34310804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33971995-G-A

34313194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33970127-T-C

34313331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33970000-A-G

34313381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33969919-G-A

34313421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33969849-G-T

34313505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33969762-C-T

34313561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33969714-T-A

34314786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33968310-T-C

34314898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33968194-C-T

34314987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33968100-A-G

34314999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33968088-A-G

34315007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33968080-T-C

34315106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33967976-C-T

34315250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33967844-T-G

34316036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33966964-G-A

34316308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33966740-C-T

34316433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33966636-C-T

34316454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33966615-C-T

34316526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33966541-T-C

34316834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33966301-G-A

34316971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33966208-C-T

34317666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33965558-C-T

34317882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33965344-G-A

34318057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33965187-G-A

34318366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33964922-A-T

34318845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33964424-C-T

34319504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33963686-T-C

34319772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33963291-G-A

34319772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33963291-G-T

34319928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33963152-A-G

http://identifiers.org/hco/19/GRCh38#34319961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33963119-C-A

34319961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33963119-C-T

34320003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33963077-G-A

34320003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33963077-G-C

http://identifiers.org/hco/19/GRCh38#34320154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33962967-A-C

http://identifiers.org/hco/19/GRCh38#34320197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33962924-A-C

34320213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33962907-G-T

34321983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

34323477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33960010-C-G

34323542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33959964-A-G

http://identifiers.org/hco/19/GRCh38#34323917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33959699-C-A

34324101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33959531-C-T

34325129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33959087-T-G

34325156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33959061-C-T

34325168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33959049-T-C

34325323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33958911-C-G

34325697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33958559-G-A

34325782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33958487-C-T

http://identifiers.org/hco/19/GRCh38#34325839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33958429-C-A

34325839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33958429-C-T

34325875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33958396-C-T

34325892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33958379-A-T

34325959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33958320-G-C

34326154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33958076-G-T

34326176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33958055-G-T

34327374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33957624-G-A

34327374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33957624-G-T

34327381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33957616-A-G

34327413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 33957584-T-C

34327454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33957543-G-T

34327469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33957528-A-G

34327630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33957358-T-C

34327675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33957301-A-T

34327771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 33957150-G-C

34327870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33957051-C-T

34327954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33956967-G-A

34328035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 33956886-A-G

34328220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33956694-G-A

34328220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33956694-G-T

34328225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33956689-G-A

34328225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33956689-G-T

34328252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33956660-G-A

34328252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33956660-G-T

34330123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33956066-T-A

34330291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33955891-A-G

34330300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33955882-G-A

34332667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33954596-A-G

34332722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33954542-G-C

34332820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33954418-C-T

34333254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33953836-G-A

34333254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33953836-G-C

34333430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33953744-C-T

34333572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33953635-T-C

34333644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33953547-A-T

34333675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33953522-T-A

34333675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33953522-T-C

34333675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33953522-T-G

34333725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33953486-A-G

34333725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33953486-A-T

http://identifiers.org/hco/19/GRCh38#34333906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33953334-C-A

34333906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33953334-C-T

34333928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33953312-T-C

34334054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33953199-C-T

34334118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33953140-C-G

34340012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33947480-A-G

34340311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33947205-T-C

34341386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33945428-T-C

34341389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33945425-T-C

http://identifiers.org/hco/19/GRCh38#34341549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33945277-C-A

34341549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 33945277-C-T

34341567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33945259-A-G

34341915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33944929-T-A

http://identifiers.org/hco/19/GRCh38#34342002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33944842-C-A

34342490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33944354-A-G

34346495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33943893-T-C

34347309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33942438-C-T

34347330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33942424-T-A

34347380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33942375-G-A

34347710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33941985-C-T

http://identifiers.org/hco/19/GRCh38#34347782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33941920-C-A

34347945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33941760-G-A

34347945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33941760-G-C

http://identifiers.org/hco/19/GRCh38#34347987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33941718-C-A

34347987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 33941718-C-T

34348095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33941611-A-G

http://identifiers.org/hco/19/GRCh38#34348255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33941480-C-A

34348255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33941480-C-T

http://identifiers.org/hco/19/GRCh38#34348259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33941476-C-A

34348259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33941476-C-T

34348279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33941456-T-G

http://identifiers.org/hco/19/GRCh38#34348286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33941451-A-C

34348286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33941451-A-G

34348956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33940128-G-A

34348956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33940128-G-C

34348956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33940128-G-T

34348958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33940126-G-A

34349021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33940064-G-A

34349214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33939892-T-C

http://identifiers.org/hco/19/GRCh38#34349274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33939849-C-A

34349274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33939849-C-T

34349278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33939845-T-C

34351456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33939291-A-G

34351546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33939213-C-G

34351546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33939213-C-T

34351642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33939143-G-A

34351642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33939143-G-T

34352641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 33938666-T-C

34352699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33938608-C-T

34352724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 33938583-C-T

http://identifiers.org/hco/19/GRCh38#34352811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33938496-C-A

34352811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 33938496-C-T

http://identifiers.org/hco/19/GRCh38#34352997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33938329-C-A

34352997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33938329-C-T

34353004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33938322-G-A

34353004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33938322-G-T

34353008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33938318-G-A

34353008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33938318-G-T

34353027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33938304-A-G

http://identifiers.org/hco/19/GRCh38#34353179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33938145-C-A

34353494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33937848-T-G

http://identifiers.org/hco/19/GRCh38#34353696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33937662-C-A

http://identifiers.org/hco/19/GRCh38#34353775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#33937610-C-A

34353775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33937610-C-T

34353794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33937586-G-A

34353794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33937586-G-T

34353872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33937497-C-T

34355216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29016
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 33936460-T-C