48986449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 73563724-A-G

48986449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 73563724-A-T

48986545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73563793-G-T

48986578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73563820-G-T

http://identifiers.org/hco/4/GRCh38#48986580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73563822-C-A

48986580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73563822-C-T

48986647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73563878-A-G

48986664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73563896-G-A

48986664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73563896-G-C

48986664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73563896-G-T

http://identifiers.org/hco/4/GRCh38#48986682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73563914-C-A

48986682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73563914-C-T

http://identifiers.org/hco/4/GRCh38#48986724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73563930-C-A

48986724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73563930-C-T

48986749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73563947-G-A

48986751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73563949-A-G

http://identifiers.org/hco/4/GRCh38#48986805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73563984-C-A

48986817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73563996-T-A

48986817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73563996-T-C

http://identifiers.org/hco/4/GRCh38#48986904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73564064-C-A

48986989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 73564153-A-G

48987129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73564291-G-T

48987192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73564354-C-T

http://identifiers.org/hco/4/GRCh38#48987205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73564367-A-C

48987247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73564416-G-A

48987253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73564423-A-G

48987580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73564649-T-C

48987591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73564660-C-T

48987708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73564776-T-G

48987867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73564905-G-A

http://identifiers.org/hco/4/GRCh38#48987983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73565017-C-A

http://identifiers.org/hco/4/GRCh38#48988043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73565098-A-C

48988043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73565098-A-G

48988056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73565111-A-G

48988395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73565409-G-A

48988395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73565409-G-T

48988459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73565468-C-T

48988667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 73565670-T-C

48988730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73565812-G-A

48988756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73565897-T-C

48988791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73565987-T-C

48988840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73566036-C-G

48988878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73566070-A-G

http://identifiers.org/hco/4/GRCh38#48989575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73567319-C-A

48989575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73567319-C-T

48990006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73567600-G-A

48990325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73568176-T-C

48990331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73568182-C-T

48990649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73568449-C-T

48990734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73568532-T-C

48990747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73568545-T-C

48990883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73568677-C-T

48990964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73568755-A-G

48991013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73568804-G-A

48991085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73568879-A-G

48991129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73568917-G-A

48991270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73569031-A-G

48991315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73569075-A-T

48991528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 73569269-C-G

48991535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 73569276-T-G

http://identifiers.org/hco/4/GRCh38#48991642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73569382-C-A

48991642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73569382-C-T

http://identifiers.org/hco/4/GRCh38#48991717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73569423-C-A

48991828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73570247-T-C

http://identifiers.org/hco/4/GRCh38#48991846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73570265-A-C

48991846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73570265-A-G

http://identifiers.org/hco/4/GRCh38#48991857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73570276-C-A

48991857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73570276-C-T

48992011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 73570428-C-T

48992044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 73570461-G-A

48992099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73570516-G-C

48993343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73571330-C-G

48993471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73571473-G-A

48993590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73571589-T-C

48993599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73571598-G-A

48993600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73571599-T-C

48993605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73571604-A-G

48993696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73571711-G-T

48994094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73571797-T-C

48994104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73571807-C-T

48994179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73571862-T-C

48994186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73571869-C-T

48994237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73571919-C-T

48994292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73571973-C-T

48994363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73572062-C-T

http://identifiers.org/hco/4/GRCh38#48994479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73572169-A-C

48994479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73572169-A-G

48994479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73572169-A-T

48994493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73572175-T-C

48994531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73572213-A-T

http://identifiers.org/hco/4/GRCh38#48994539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73572225-C-A

48994649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 73572305-A-G

48994668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 73572324-G-A

48998060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73573738-G-A

48998092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73573772-G-A

48998313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73573932-T-C

48998360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73573955-C-T

http://identifiers.org/hco/4/GRCh38#48998457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73574048-C-A

48998461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: 73574052-G-A

48998466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 73574057-A-G

48998518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 73574109-C-T

48998519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 73574110-G-A

48998552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73574143-T-A

48998552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73574143-T-C

48998552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73574143-T-G

49003225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73574783-T-C

49003494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73575033-T-G

http://identifiers.org/hco/4/GRCh38#49003572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73575107-C-A

49004002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73575555-T-C

http://identifiers.org/hco/4/GRCh38#49004062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73575611-A-C

49006063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73577363-T-G

49006221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73577503-A-G

49006275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73577554-C-T

49006364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73577624-A-T

http://identifiers.org/hco/4/GRCh38#49006462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73577714-A-C

49007190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73578786-T-C

49007343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73578941-A-G

49017229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73581238-T-C

49017239-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73581248-T-A

49017239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73581248-T-G

http://identifiers.org/hco/4/GRCh38#49017251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73581260-C-A

49017278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 73581287-T-C

49017278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73581287-T-G

49017307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 73581316-T-C

49017313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 73581322-A-G

49017319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 73581328-G-A

49017321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73581330-G-A

49017347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73581355-T-C

http://identifiers.org/hco/4/GRCh38#49017403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73583431-C-A

49017403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73583431-C-G

http://identifiers.org/hco/4/GRCh38#49017413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73583448-C-A

49017413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73583448-C-G

http://identifiers.org/hco/4/GRCh38#49017419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73583454-C-A

49017419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73583454-C-T

49017439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73583474-G-A

49017439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73583474-G-C

49017439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73583474-G-T

49017440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73583475-G-A

http://identifiers.org/hco/4/GRCh38#49017450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73583484-C-A

49017452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73583486-T-A

49017452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73583486-T-C

49017452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73583486-T-G

49017588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73583582-T-G

49018427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73583624-G-T

49018456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73583653-A-G

49018501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73583703-A-G

http://identifiers.org/hco/4/GRCh38#49018521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73583723-C-A

49018521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73583723-C-T

49018858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73584033-G-T

49018900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73584071-T-C

49018923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73584104-C-T

http://identifiers.org/hco/4/GRCh38#49018936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73584118-C-A

49018936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73584118-C-T

49018964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73584146-A-G

49019014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73584195-A-G

49019201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73584366-G-T

49019240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73584408-C-G

49019306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73584465-T-C

49019329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73584495-G-T

49019330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73584496-A-G

49019392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73584561-G-A

49019457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73584621-G-A

49019505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73584674-A-G

http://identifiers.org/hco/4/GRCh38#49028488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73585768-C-A

49028558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73585839-G-A

49028558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73585839-G-T

49028585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73585865-A-G

49028637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 73585918-C-G

49028637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 73585918-C-T

49028649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 73585930-T-C

49028746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586031-T-A

49028752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586037-T-C

49028773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586058-T-A

49028773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586058-T-C

49028784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586069-C-T

49028792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586077-T-C

49028802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586087-T-C

49028805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586090-T-C

49028805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586090-T-G

49028806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586091-A-G

49028879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586134-T-A

49028929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586173-G-A

49028969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586208-A-G

49028975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586214-C-T

49030168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586585-A-G

49030242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586653-C-T

49030281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586691-C-T

49030291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586701-T-C

49030391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586773-G-A

49030391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586773-G-T

http://identifiers.org/hco/4/GRCh38#49030461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73586845-C-A

49030461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73586845-C-T

49030523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73587139-T-A

http://identifiers.org/hco/4/GRCh38#49030806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73587728-C-A

49030806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 73587728-C-T

49030871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 73587801-T-C

49030910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73587840-G-C

49030910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 73587840-G-T

49030974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73587904-G-T

49030978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73587908-G-A

http://identifiers.org/hco/4/GRCh38#49030985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73587914-C-A

49030987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73587916-G-A

49031067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73587976-G-C

49031067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73587976-G-T

49031136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73588039-T-C

49031166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73588064-T-A

http://identifiers.org/hco/4/GRCh38#49031197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73588098-C-A

49031197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73588098-C-T

49031215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73588107-G-A

49031215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73588107-G-T

http://identifiers.org/hco/4/GRCh38#49031247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73588139-C-A

49031247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 73588139-C-T

49032322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73588928-T-C

http://identifiers.org/hco/4/GRCh38#49032432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73589038-C-A

49032432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73589038-C-T

49032447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73589056-T-C

49032447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73589056-T-G

49032528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73589135-T-G

49032531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73589138-C-G

49032583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 73589184-G-A

49032583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 73589184-G-T

49032666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 73589267-A-G

49032826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73589454-A-G

http://identifiers.org/hco/4/GRCh38#49032837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73589465-C-A

49032837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73589465-C-G

49032837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73589465-C-T

49033008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73589584-G-A

49033147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73589723-C-T

49036591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73590002-A-T

49036878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73590256-G-T

49036911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73590317-T-G

49037061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73590538-A-G

49037108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73590585-G-C

49037114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73590591-C-T

49037135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73590611-T-C

49037138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73590614-T-G

49037177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73590656-C-T

49037233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73590709-G-A

49037295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73590771-G-A

49037296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73590772-C-T

49037297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73590773-G-A

49037783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73591323-T-A

49037922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73591452-A-G

http://identifiers.org/hco/4/GRCh38#49037974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73591504-C-A

49038072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 73591603-T-C

49038135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 73591666-T-C

http://identifiers.org/hco/4/GRCh38#49038273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73591800-C-A

49043500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73594520-G-C

49043793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73594773-C-G

49043849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73594837-A-G

49043938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73594916-C-T

49044232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73595196-T-C

49044406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73595415-G-A

http://identifiers.org/hco/4/GRCh38#49044594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73595573-C-A

49044594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73595573-C-T

49044595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73595574-G-A

49044666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73595644-A-T

49044732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73595724-G-C

49044732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73595724-G-T

49044770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73595762-C-G

49044770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73595762-C-T

49044772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73595764-C-T

49044860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73595852-G-A

49044860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73595852-G-T

49044930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73595902-T-C

http://identifiers.org/hco/4/GRCh38#49049137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73597312-C-A

49049137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73597312-C-T

49049221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73597387-C-T

49049376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73597504-G-A

49049376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73597504-G-T

49049443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73597557-C-T

49049463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73597570-C-T

49049835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73597801-A-G

49049879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73597828-T-A

49049879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73597828-T-G

49049982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73597929-C-T

49050020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73597952-A-G

49050028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73597960-C-T

49050147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73598070-C-T

49050395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73598329-A-G

49050472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73598405-G-T

http://identifiers.org/hco/4/GRCh38#49050526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73598454-A-C

49050533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73598461-G-T

49050572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73598500-T-G

http://identifiers.org/hco/4/GRCh38#49050579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73598507-C-A

49050579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73598507-C-T

49050599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73598527-G-T

http://identifiers.org/hco/4/GRCh38#49050615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73598543-C-A

49050621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73598549-G-A

49050621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73598549-G-T

49050667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73598621-T-A

49050687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 73598641-G-A

49050687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 73598641-G-C

49050803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 73598757-G-C

49050803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 73598757-G-T

49050857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 73598827-C-T

http://identifiers.org/hco/4/GRCh38#49050890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73598861-C-A

49050890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73598861-C-T

http://identifiers.org/hco/4/GRCh38#49050893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73598864-C-A

49050893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73598864-C-T

49050925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73598895-G-T

49050967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73598937-A-G

49050967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73598937-A-T

http://identifiers.org/hco/4/GRCh38#49050991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73598961-A-C

49051094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73599131-T-C

http://identifiers.org/hco/4/GRCh38#49051100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73599137-A-C

49051195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73599256-C-G

49051195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73599256-C-T

49051217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73599278-G-A

49052019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73599762-T-G

49052633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73605358-T-G

49052652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73605377-C-T

http://identifiers.org/hco/4/GRCh38#49052734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73605452-A-C

49052739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73605456-A-G

49052817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73605490-T-C

http://identifiers.org/hco/4/GRCh38#49052933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#73605557-C-A

49052994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73605626-G-C

49060722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73610056-T-C

49060787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73610121-C-G

49061754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73610308-A-G

49061759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73610316-T-A

49061759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73610316-T-C

49061769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 73610326-T-C

49061905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73610454-G-A

49061905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73610454-G-T

49061907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73610456-A-T

49061917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73610461-T-C

49062018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26133
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 73610558-T-C